Canonical Allele Identifier: CA786428199

Gene: FGF2

Linked Data

• dbSNP Id: rs1330830246
• MyVariant Identifiers: chr4:g.123772673G>A (hg19) ; chr4:g.122851518G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122851518G>A , CM000666.2:g.122851518G>A	GRCh38
NC_000004.11:g.123772673G>A , CM000666.1:g.123772673G>A	GRCh37
NC_000004.10:g.123992123G>A	NCBI36
NG_029067.1:g.29811G>A
NG_029067.2:g.29811G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264498.9:c.577+24166G>A	ENSP00000264498.4:n.577+24166G>A
ENST00000264498.8:c.577+24166G>A	ENSP00000264498.4:n.577+24166G>A
ENST00000644866.2:c.178+24166G>A MANE Select	ENSP00000494222.1:n.178+24166G>A
ENST00000264498.7:c.577+24166G>A	ENSP00000264498.3:n.577+24166G>A
ENST00000608478.1:c.178+24166G>A	ENSP00000477134.1:n.178+24166G>A
ENST00000614010.4:c.577+24166G>A	ENSP00000478620.1:n.577+24166G>A
NM_002006.4:c.577+24166G>A	NP_001997.5:n.577+24166G>A
NM_001361665.1:c.178+24166G>A	NP_001348594.1:n.178+24166G>A
NM_002006.5:c.577+24166G>A	NP_001997.5:n.577+24166G>A
NM_001361665.2:c.178+24166G>A MANE Select	NP_001348594.1:n.178+24166G>A
NM_002006.6:c.577+24166G>A	NP_001997.5:n.577+24166G>A