Canonical Allele Identifier: CA1941060902

Gene: FGFR2

Linked Data

• dbSNP Id: rs1863159968

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121594562C>T , CM000672.2:g.121594562C>T	GRCh38
NC_000010.10:g.123354076C>T , CM000672.1:g.123354076C>T	GRCh37
NC_000010.9:g.123344066C>T	NCBI36
NG_012449.1:g.8897G>A
NG_012449.2:g.8897G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.-150-595G>A MANE Plus Clinical	ENSP00000410294.2:n.-150-595G>A
ENST00000351936.11:c.-158G>A	ENSP00000309878.10:n.-158G>A
ENST00000682550.1:c.-150-595G>A	ENSP00000507633.1:n.-150-595G>A
ENST00000683035.1:c.-745G>A	ENSP00000507074.1:n.-745G>A
ENST00000683211.1:c.-745G>A	ENSP00000508257.1:n.-745G>A
ENST00000684153.1:c.-150-595G>A	ENSP00000506937.1:n.-150-595G>A
ENST00000358487.10:c.-150-595G>A MANE Select	ENSP00000351276.6:n.-150-595G>A
ENST00000636922.1:c.-150-595G>A	ENSP00000490905.1:n.-150-595G>A
ENST00000336553.10:c.-150-595G>A	ENSP00000337665.6:n.-150-595G>A
ENST00000356226.8:c.-150-595G>A	ENSP00000348559.4:n.-150-595G>A
ENST00000357555.9:c.-150-595G>A	ENSP00000350166.5:n.-150-595G>A
ENST00000358487.9:c.-150-595G>A	ENSP00000351276.5:n.-150-595G>A
ENST00000359354.6:c.-150-595G>A	ENSP00000352309.2:n.-150-595G>A
ENST00000360144.7:c.-150-595G>A	ENSP00000353262.3:n.-150-595G>A
ENST00000369058.7:c.-150-595G>A	ENSP00000358054.3:n.-150-595G>A
ENST00000369059.5:c.-150-595G>A	ENSP00000358055.1:n.-150-595G>A
ENST00000369060.8:c.-150-595G>A	ENSP00000358056.4:n.-150-595G>A
ENST00000457416.6:c.-150-595G>A	ENSP00000410294.2:n.-150-595G>A
ENST00000490349.5:n.112-595G>A
ENST00000604236.5:c.-150-595G>A	ENSP00000474109.1:n.-150-595G>A
ENST00000613048.4:c.-150-595G>A	ENSP00000484154.1:n.-150-595G>A
NM_000141.4:c.-150-595G>A	NP_000132.3:n.-150-595G>A
NM_001144915.1:c.-150-595G>A	NP_001138387.1:n.-150-595G>A
NM_001144917.1:c.-150-595G>A	NP_001138389.1:n.-150-595G>A
NM_001144918.1:c.-150-595G>A	NP_001138390.1:n.-150-595G>A
NM_001144919.1:c.-150-595G>A	NP_001138391.1:n.-150-595G>A
NM_022970.3:c.-150-595G>A	NP_075259.4:n.-150-595G>A
NR_073009.1:n.498-595G>A
XM_006717708.2:c.-93-595G>A	XP_006717771.1:n.-93-595G>A
XM_006717709.2:c.-93-595G>A	XP_006717772.1:n.-93-595G>A
XM_006717710.2:c.-93-595G>A	XP_006717773.1:n.-93-595G>A
XM_006717713.2:c.-93-595G>A	XP_006717776.1:n.-93-595G>A
NM_001320658.1:c.-150-595G>A	NP_001307587.1:n.-150-595G>A
XM_006717708.3:c.-93-595G>A	XP_006717771.1:n.-93-595G>A
XM_006717710.4:c.-93-595G>A	XP_006717773.1:n.-93-595G>A
XM_017015920.2:c.-93-595G>A	XP_016871409.1:n.-93-595G>A
XM_017015921.2:c.-93-595G>A	XP_016871410.1:n.-93-595G>A
XM_017015924.2:c.-93-595G>A	XP_016871413.1:n.-93-595G>A
XM_017015925.2:c.-93-595G>A	XP_016871414.1:n.-93-595G>A
XM_024447887.1:c.-93-595G>A	XP_024303655.1:n.-93-595G>A
XM_024447888.1:c.-93-595G>A	XP_024303656.1:n.-93-595G>A
XM_024447889.1:c.-93-595G>A	XP_024303657.1:n.-93-595G>A
XM_024447890.1:c.-93-595G>A	XP_024303658.1:n.-93-595G>A
XM_024447891.1:c.-93-595G>A	XP_024303659.1:n.-93-595G>A
NM_000141.5:c.-150-595G>A MANE Select	NP_000132.3:n.-150-595G>A
NM_001144917.2:c.-150-595G>A	NP_001138389.1:n.-150-595G>A
NM_001144918.2:c.-150-595G>A	NP_001138390.1:n.-150-595G>A
NM_001144919.2:c.-150-595G>A	NP_001138391.1:n.-150-595G>A
NM_001320658.2:c.-150-595G>A	NP_001307587.1:n.-150-595G>A
NR_073009.2:n.484-595G>A
NM_001144915.2:c.-150-595G>A	NP_001138387.1:n.-150-595G>A