Canonical Allele Identifier: CA471647221

Gene: FGFR2

Linked Data

• dbSNP Id: rs1451945582
• gnomAD v2: 10-123247523-A-G
• gnomAD v4: 10-121488009-A-G
• MyVariant Identifiers: chr10:g.123247523A>G (hg19) ; chr10:g.121488009A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488009A>G , CM000672.2:g.121488009A>G	GRCh38
NC_000010.10:g.123247523A>G , CM000672.1:g.123247523A>G	GRCh37
NC_000010.9:g.123237513A>G	NCBI36
NG_012449.1:g.115450T>C
NG_012449.2:g.115450T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000457416.7:c.1971T>C MANE Plus Clinical	ENSP00000410294.2:p.Tyr657=
ENST00000351936.11:c.1962T>C	ENSP00000309878.10:p.Tyr654=
ENST00000638709.2:c.792T>C	ENSP00000491912.2:p.Tyr264=
ENST00000682296.1:n.1310T>C
ENST00000682550.1:c.1617T>C	ENSP00000507633.1:p.Tyr539=
ENST00000682772.1:c.792T>C	ENSP00000506848.1:p.Tyr264=
ENST00000682904.1:n.788T>C
ENST00000683029.1:n.380T>C
ENST00000683211.1:c.1962T>C	ENSP00000508257.1:p.Tyr654=
ENST00000683250.1:c.*670T>C	ENSP00000506847.1:n.*670T>C
ENST00000683418.1:n.4309T>C
ENST00000684153.1:c.1617T>C	ENSP00000506937.1:p.Tyr539=
ENST00000684516.1:n.2981T>C
ENST00000358487.10:c.1968T>C MANE Select	ENSP00000351276.6:p.Tyr656=
ENST00000336553.10:c.1695T>C	ENSP00000337665.6:p.Tyr565=
ENST00000346997.6:c.1962T>C	ENSP00000263451.5:p.Tyr654=
ENST00000351936.10:c.1968T>C	ENSP00000309878.9:p.Tyr656=
ENST00000356226.8:c.1617T>C	ENSP00000348559.4:p.Tyr539=
ENST00000357555.9:c.1701T>C	ENSP00000350166.5:p.Tyr567=
ENST00000358487.9:c.1968T>C	ENSP00000351276.5:p.Tyr656=
ENST00000360144.7:c.1704T>C	ENSP00000353262.3:p.Tyr568=
ENST00000369056.5:c.1971T>C	ENSP00000358052.1:p.Tyr657=
ENST00000369058.7:c.1971T>C	ENSP00000358054.3:p.Tyr657=
ENST00000369059.5:c.1626T>C	ENSP00000358055.1:p.Tyr542=
ENST00000369060.8:c.1620T>C	ENSP00000358056.4:p.Tyr540=
ENST00000369061.8:c.1632T>C	ENSP00000358057.4:p.Tyr544=
ENST00000429361.5:c.744T>C	ENSP00000404219.1:p.Tyr248=
ENST00000457416.6:c.1971T>C	ENSP00000410294.2:p.Tyr657=
ENST00000478859.5:c.1284T>C	ENSP00000474011.1:p.Tyr428=
ENST00000604236.5:c.*1015T>C	ENSP00000474109.1:n.*1015T>C
ENST00000613048.4:c.1701T>C	ENSP00000484154.1:p.Tyr567=
NM_000141.4:c.1968T>C	NP_000132.3:p.Tyr656=
NM_001144913.1:c.1971T>C	NP_001138385.1:p.Tyr657=
NM_001144914.1:c.1632T>C	NP_001138386.1:p.Tyr544=
NM_001144915.1:c.1701T>C	NP_001138387.1:p.Tyr567=
NM_001144916.1:c.1623T>C	NP_001138388.1:p.Tyr541=
NM_001144917.1:c.1620T>C	NP_001138389.1:p.Tyr540=
NM_001144918.1:c.1617T>C	NP_001138390.1:p.Tyr539=
NM_001144919.1:c.1704T>C	NP_001138391.1:p.Tyr568=
NM_022970.3:c.1971T>C	NP_075259.4:p.Tyr657=
NM_023029.2:c.1701T>C	NP_075418.1:p.Tyr567=
NR_073009.1:n.2418T>C
XM_006717708.2:c.2022T>C	XP_006717771.1:p.Tyr674=
XM_006717709.2:c.2019T>C	XP_006717772.1:p.Tyr673=
XM_006717710.2:c.2028T>C	XP_006717773.1:p.Tyr676=
XM_006717711.2:c.1761T>C	XP_006717774.1:p.Tyr587=
XM_006717712.2:c.1683T>C	XP_006717775.1:p.Tyr561=
XM_006717713.2:c.2025T>C	XP_006717776.1:p.Tyr675=
XM_011539510.1:c.1284T>C	XP_011537812.1:p.Tyr428=
NM_001320654.1:c.1284T>C	NP_001307583.1:p.Tyr428=
NM_001320658.1:c.1962T>C	NP_001307587.1:p.Tyr654=
XM_006717708.3:c.2022T>C	XP_006717771.1:p.Tyr674=
XM_006717710.4:c.2028T>C	XP_006717773.1:p.Tyr676=
XM_017015920.2:c.2022T>C	XP_016871409.1:p.Tyr674=
XM_017015921.2:c.2019T>C	XP_016871410.1:p.Tyr673=
XM_017015924.2:c.1680T>C	XP_016871413.1:p.Tyr560=
XM_017015925.2:c.1674T>C	XP_016871414.1:p.Tyr558=
XM_024447887.1:c.1758T>C	XP_024303655.1:p.Tyr586=
XM_024447888.1:c.1755T>C	XP_024303656.1:p.Tyr585=
XM_024447889.1:c.1752T>C	XP_024303657.1:p.Tyr584=
XM_024447890.1:c.1761T>C	XP_024303658.1:p.Tyr587=
XM_024447891.1:c.1683T>C	XP_024303659.1:p.Tyr561=
XM_024447892.1:c.798T>C	XP_024303660.1:p.Tyr266=
NM_000141.5:c.1968T>C MANE Select	NP_000132.3:p.Tyr656=
NM_001144917.2:c.1620T>C	NP_001138389.1:p.Tyr540=
NM_001144918.2:c.1617T>C	NP_001138390.1:p.Tyr539=
NM_001144919.2:c.1704T>C	NP_001138391.1:p.Tyr568=
NM_001320658.2:c.1962T>C	NP_001307587.1:p.Tyr654=
NR_073009.2:n.2404T>C
NM_001144915.2:c.1701T>C	NP_001138387.1:p.Tyr567=
NM_001144916.2:c.1623T>C	NP_001138388.1:p.Tyr541=
NM_001320654.2:c.1284T>C	NP_001307583.1:p.Tyr428=