Canonical Allele Identifier: CA105260893

Gene: FGF2

Linked Data

• dbSNP Id: rs369105783
• MyVariant Identifiers: chr4:g.123772694T>G (hg19) ; chr4:g.122851539T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122851539T>G , CM000666.2:g.122851539T>G	GRCh38
NC_000004.11:g.123772694T>G , CM000666.1:g.123772694T>G	GRCh37
NC_000004.10:g.123992144T>G	NCBI36
NG_029067.1:g.29832T>G
NG_029067.2:g.29832T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264498.9:c.577+24187T>G	ENSP00000264498.4:n.577+24187T>G
ENST00000264498.8:c.577+24187T>G	ENSP00000264498.4:n.577+24187T>G
ENST00000644866.2:c.178+24187T>G MANE Select	ENSP00000494222.1:n.178+24187T>G
ENST00000264498.7:c.577+24187T>G	ENSP00000264498.3:n.577+24187T>G
ENST00000608478.1:c.178+24187T>G	ENSP00000477134.1:n.178+24187T>G
ENST00000614010.4:c.577+24187T>G	ENSP00000478620.1:n.577+24187T>G
NM_002006.4:c.577+24187T>G	NP_001997.5:n.577+24187T>G
NM_001361665.1:c.178+24187T>G	NP_001348594.1:n.178+24187T>G
NM_002006.5:c.577+24187T>G	NP_001997.5:n.577+24187T>G
NM_001361665.2:c.178+24187T>G MANE Select	NP_001348594.1:n.178+24187T>G
NM_002006.6:c.577+24187T>G	NP_001997.5:n.577+24187T>G