Canonical Allele Identifier: CA16199487
Gene: FGF2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11938826

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122851459C>G , CM000666.2:g.122851459C>G GRCh38
NC_000004.10:g.123992064C>G NCBI36
NC_000004.11:g.123772614C>G , CM000666.1:g.123772614C>G GRCh37
NG_029067.1:g.29752C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264498.7:c.577+24107C>G ENSP00000264498.3:p.=
ENST00000608478.1:c.178+24107C>G ENSP00000477134.1:p.=
ENST00000614010.4:c.577+24107C>G ENSP00000478620.1:p.=
NM_002006.4:c.577+24107C>G VV NP_001997.5:p.=