Canonical Allele Identifier: CA378315067

Gene: FGFR2

Linked Data

• dbSNP Id: rs2133839288
• MyVariant Identifiers: chr10:g.123247615C>G (hg19) ; chr10:g.121488101C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488101C>G , CM000672.2:g.121488101C>G	GRCh38
NC_000010.10:g.123247615C>G , CM000672.1:g.123247615C>G	GRCh37
NC_000010.9:g.123237605C>G	NCBI36
NG_012449.1:g.115358G>C
NG_012449.2:g.115358G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000457416.7:c.1879G>C MANE Plus Clinical	ENSP00000410294.2:p.Asp627His
ENST00000351936.11:c.1870G>C	ENSP00000309878.10:p.Asp624His
ENST00000638709.2:c.700G>C	ENSP00000491912.2:p.Asp234His
ENST00000682296.1:n.1218G>C
ENST00000682550.1:c.1525G>C	ENSP00000507633.1:p.Asp509His
ENST00000682772.1:c.700G>C	ENSP00000506848.1:p.Asp234His
ENST00000682904.1:n.696G>C
ENST00000683029.1:n.288G>C
ENST00000683211.1:c.1870G>C	ENSP00000508257.1:p.Asp624His
ENST00000683250.1:c.*578G>C	ENSP00000506847.1:n.*578G>C
ENST00000683418.1:n.4217G>C
ENST00000684153.1:c.1525G>C	ENSP00000506937.1:p.Asp509His
ENST00000684516.1:n.2889G>C
ENST00000358487.10:c.1876G>C MANE Select	ENSP00000351276.6:p.Asp626His
ENST00000336553.10:c.1603G>C	ENSP00000337665.6:p.Asp535His
ENST00000346997.6:c.1870G>C	ENSP00000263451.5:p.Asp624His
ENST00000351936.10:c.1876G>C	ENSP00000309878.9:p.Asp626His
ENST00000356226.8:c.1525G>C	ENSP00000348559.4:p.Asp509His
ENST00000357555.9:c.1609G>C	ENSP00000350166.5:p.Asp537His
ENST00000358487.9:c.1876G>C	ENSP00000351276.5:p.Asp626His
ENST00000360144.7:c.1612G>C	ENSP00000353262.3:p.Asp538His
ENST00000369056.5:c.1879G>C	ENSP00000358052.1:p.Asp627His
ENST00000369058.7:c.1879G>C	ENSP00000358054.3:p.Asp627His
ENST00000369059.5:c.1534G>C	ENSP00000358055.1:p.Asp512His
ENST00000369060.8:c.1528G>C	ENSP00000358056.4:p.Asp510His
ENST00000369061.8:c.1540G>C	ENSP00000358057.4:p.Asp514His
ENST00000429361.5:c.652G>C	ENSP00000404219.1:p.Asp218His
ENST00000457416.6:c.1879G>C	ENSP00000410294.2:p.Asp627His
ENST00000478859.5:c.1192G>C	ENSP00000474011.1:p.Asp398His
ENST00000604236.5:c.*923G>C	ENSP00000474109.1:n.*923G>C
ENST00000613048.4:c.1609G>C	ENSP00000484154.1:p.Asp537His
NM_000141.4:c.1876G>C	NP_000132.3:p.Asp626His
NM_001144913.1:c.1879G>C	NP_001138385.1:p.Asp627His
NM_001144914.1:c.1540G>C	NP_001138386.1:p.Asp514His
NM_001144915.1:c.1609G>C	NP_001138387.1:p.Asp537His
NM_001144916.1:c.1531G>C	NP_001138388.1:p.Asp511His
NM_001144917.1:c.1528G>C	NP_001138389.1:p.Asp510His
NM_001144918.1:c.1525G>C	NP_001138390.1:p.Asp509His
NM_001144919.1:c.1612G>C	NP_001138391.1:p.Asp538His
NM_022970.3:c.1879G>C	NP_075259.4:p.Asp627His
NM_023029.2:c.1609G>C	NP_075418.1:p.Asp537His
NR_073009.1:n.2326G>C
XM_006717708.2:c.1930G>C	XP_006717771.1:p.Asp644His
XM_006717709.2:c.1927G>C	XP_006717772.1:p.Asp643His
XM_006717710.2:c.1936G>C	XP_006717773.1:p.Asp646His
XM_006717711.2:c.1669G>C	XP_006717774.1:p.Asp557His
XM_006717712.2:c.1591G>C	XP_006717775.1:p.Asp531His
XM_006717713.2:c.1933G>C	XP_006717776.1:p.Asp645His
XM_011539510.1:c.1192G>C	XP_011537812.1:p.Asp398His
NM_001320654.1:c.1192G>C	NP_001307583.1:p.Asp398His
NM_001320658.1:c.1870G>C	NP_001307587.1:p.Asp624His
XM_006717708.3:c.1930G>C	XP_006717771.1:p.Asp644His
XM_006717710.4:c.1936G>C	XP_006717773.1:p.Asp646His
XM_017015920.2:c.1930G>C	XP_016871409.1:p.Asp644His
XM_017015921.2:c.1927G>C	XP_016871410.1:p.Asp643His
XM_017015924.2:c.1588G>C	XP_016871413.1:p.Asp530His
XM_017015925.2:c.1582G>C	XP_016871414.1:p.Asp528His
XM_024447887.1:c.1666G>C	XP_024303655.1:p.Asp556His
XM_024447888.1:c.1663G>C	XP_024303656.1:p.Asp555His
XM_024447889.1:c.1660G>C	XP_024303657.1:p.Asp554His
XM_024447890.1:c.1669G>C	XP_024303658.1:p.Asp557His
XM_024447891.1:c.1591G>C	XP_024303659.1:p.Asp531His
XM_024447892.1:c.706G>C	XP_024303660.1:p.Asp236His
NM_000141.5:c.1876G>C MANE Select	NP_000132.3:p.Asp626His
NM_001144917.2:c.1528G>C	NP_001138389.1:p.Asp510His
NM_001144918.2:c.1525G>C	NP_001138390.1:p.Asp509His
NM_001144919.2:c.1612G>C	NP_001138391.1:p.Asp538His
NM_001320658.2:c.1870G>C	NP_001307587.1:p.Asp624His
NR_073009.2:n.2312G>C
NM_001144915.2:c.1609G>C	NP_001138387.1:p.Asp537His
NM_001144916.2:c.1531G>C	NP_001138388.1:p.Asp511His
NM_001320654.2:c.1192G>C	NP_001307583.1:p.Asp398His