Canonical Allele Identifier: CA2846654630

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121478331A>G , CM000672.2:g.121478331A>G	GRCh38
NC_000010.10:g.123237845A>G , CM000672.1:g.123237845A>G	GRCh37
NC_000010.9:g.123227835A>G	NCBI36
NG_012449.1:g.125128T>C
NG_012449.2:g.125128T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000141.4:c.*1526T>C	NP_000132.3:n.*1526T>C
NM_001144914.1:c.*1526T>C	NP_001138386.1:n.*1526T>C
NM_001144915.1:c.*1250T>C	NP_001138387.1:n.*1250T>C
NM_001144916.1:c.*1526T>C	NP_001138388.1:n.*1526T>C
NM_001144917.1:c.*1526T>C	NP_001138389.1:n.*1526T>C
NM_001144918.1:c.*1526T>C	NP_001138390.1:n.*1526T>C
NM_022970.3:c.*1526T>C	NP_075259.4:n.*1526T>C
NM_023029.2:c.*1526T>C	NP_075418.1:n.*1526T>C
NR_073009.1:n.4442T>C
NM_001320654.1:c.*1526T>C	NP_001307583.1:n.*1526T>C
NM_001320658.1:c.*1526T>C	NP_001307587.1:n.*1526T>C