Canonical Allele Identifier: CA1067519303

Gene: FGF2

Linked Data

• dbSNP Id: rs1726234362
• gnomAD v3: 4-122851642-G-T
• gnomAD v4: 4-122851642-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122851642G>T , CM000666.2:g.122851642G>T	GRCh38
NC_000004.11:g.123772797G>T , CM000666.1:g.123772797G>T	GRCh37
NC_000004.10:g.123992247G>T	NCBI36
NG_029067.1:g.29935G>T
NG_029067.2:g.29935G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264498.9:c.577+24290G>T	ENSP00000264498.4:n.577+24290G>T
ENST00000264498.8:c.577+24290G>T	ENSP00000264498.4:n.577+24290G>T
ENST00000644866.2:c.178+24290G>T MANE Select	ENSP00000494222.1:n.178+24290G>T
ENST00000264498.7:c.577+24290G>T	ENSP00000264498.3:n.577+24290G>T
ENST00000608478.1:c.178+24290G>T	ENSP00000477134.1:n.178+24290G>T
ENST00000614010.4:c.577+24290G>T	ENSP00000478620.1:n.577+24290G>T
NM_002006.4:c.577+24290G>T	NP_001997.5:n.577+24290G>T
NM_001361665.1:c.178+24290G>T	NP_001348594.1:n.178+24290G>T
NM_002006.5:c.577+24290G>T	NP_001997.5:n.577+24290G>T
NM_001361665.2:c.178+24290G>T MANE Select	NP_001348594.1:n.178+24290G>T
NM_002006.6:c.577+24290G>T	NP_001997.5:n.577+24290G>T