Canonical Allele Identifier: CA378358364

Gene: FGFR2

Linked Data

• dbSNP Id: rs1181427380
• gnomAD v2: 10-123239172-C-T
• gnomAD v4: 10-121479658-C-T
• MyVariant Identifiers: chr10:g.123239172C>T (hg19) ; chr10:g.121479658C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121479658C>T , CM000672.2:g.121479658C>T	GRCh38
NC_000010.10:g.123239172C>T , CM000672.1:g.123239172C>T	GRCh37
NC_000010.9:g.123229162C>T	NCBI36
NG_012449.1:g.123801G>A
NG_012449.2:g.123801G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.*199G>A MANE Plus Clinical	ENSP00000410294.2:n.*199G>A
ENST00000351936.11:c.*199G>A	ENSP00000309878.10:n.*199G>A
ENST00000638709.2:c.*199G>A	ENSP00000491912.2:n.*199G>A
ENST00000682296.1:n.2007G>A
ENST00000682550.1:c.*199G>A	ENSP00000507633.1:n.*199G>A
ENST00000682772.1:c.*199G>A	ENSP00000506848.1:n.*199G>A
ENST00000682904.1:n.1485G>A
ENST00000683029.1:n.2668G>A
ENST00000683211.1:c.*199G>A	ENSP00000508257.1:n.*199G>A
ENST00000683250.1:c.*2958G>A	ENSP00000506847.1:n.*2958G>A
ENST00000683418.1:n.5006G>A
ENST00000684153.1:c.*393G>A	ENSP00000506937.1:n.*393G>A
ENST00000684516.1:n.3678G>A
ENST00000358487.10:c.*199G>A MANE Select	ENSP00000351276.6:n.*199G>A
ENST00000638709.1:c.652G>A
ENST00000356226.8:c.*199G>A	ENSP00000348559.4:n.*199G>A
ENST00000357555.9:c.2047G>A	ENSP00000350166.5:p.Val683Ile
ENST00000358487.9:c.*199G>A	ENSP00000351276.5:n.*199G>A
ENST00000369059.5:c.*199G>A	ENSP00000358055.1:n.*199G>A
ENST00000369060.8:c.*199G>A	ENSP00000358056.4:n.*199G>A
ENST00000369061.8:c.*199G>A	ENSP00000358057.4:n.*199G>A
ENST00000478859.5:c.*199G>A	ENSP00000474011.1:n.*199G>A
ENST00000604236.5:c.*1712G>A	ENSP00000474109.1:n.*1712G>A
ENST00000613048.4:c.*199G>A	ENSP00000484154.1:n.*199G>A
NM_000141.4:c.*199G>A	NP_000132.3:n.*199G>A
NM_001144914.1:c.*199G>A	NP_001138386.1:n.*199G>A
NM_001144915.1:c.2047G>A	NP_001138387.1:p.Val683Ile
NM_001144916.1:c.*199G>A	NP_001138388.1:n.*199G>A
NM_001144917.1:c.*199G>A	NP_001138389.1:n.*199G>A
NM_001144918.1:c.*199G>A	NP_001138390.1:n.*199G>A
NM_022970.3:c.*199G>A	NP_075259.4:n.*199G>A
NM_023029.2:c.*199G>A	NP_075418.1:n.*199G>A
NR_073009.1:n.3115G>A
XM_006717708.2:c.*199G>A	XP_006717771.1:n.*199G>A
XM_006717709.2:c.*199G>A	XP_006717772.1:n.*199G>A
XM_006717711.2:c.*199G>A	XP_006717774.1:n.*199G>A
XM_006717712.2:c.*199G>A	XP_006717775.1:n.*199G>A
XM_011539510.1:c.*199G>A	XP_011537812.1:n.*199G>A
NM_001320654.1:c.*199G>A	NP_001307583.1:n.*199G>A
NM_001320658.1:c.*199G>A	NP_001307587.1:n.*199G>A
XM_006717708.3:c.*199G>A	XP_006717771.1:n.*199G>A
XM_006717710.4:c.*393G>A	XP_006717773.1:n.*393G>A
XM_017015920.2:c.*393G>A	XP_016871409.1:n.*393G>A
XM_017015921.2:c.*393G>A	XP_016871410.1:n.*393G>A
XM_017015924.2:c.*199G>A	XP_016871413.1:n.*199G>A
XM_017015925.2:c.*393G>A	XP_016871414.1:n.*393G>A
XM_024447887.1:c.*199G>A	XP_024303655.1:n.*199G>A
XM_024447888.1:c.*199G>A	XP_024303656.1:n.*199G>A
XM_024447889.1:c.*199G>A	XP_024303657.1:n.*199G>A
XM_024447890.1:c.*199G>A	XP_024303658.1:n.*199G>A
XM_024447891.1:c.*199G>A	XP_024303659.1:n.*199G>A
XM_024447892.1:c.*199G>A	XP_024303660.1:n.*199G>A
NM_000141.5:c.*199G>A MANE Select	NP_000132.3:n.*199G>A
NM_001144917.2:c.*199G>A	NP_001138389.1:n.*199G>A
NM_001144918.2:c.*199G>A	NP_001138390.1:n.*199G>A
NM_001320658.2:c.*199G>A	NP_001307587.1:n.*199G>A
NR_073009.2:n.3101G>A
NM_001144915.2:c.2047G>A	NP_001138387.1:p.Val683Ile
NM_001144916.2:c.*199G>A	NP_001138388.1:n.*199G>A
NM_001320654.2:c.*199G>A	NP_001307583.1:n.*199G>A