Canonical Allele Identifier: CA15303860
Gene: FGF2 HGNC NCBI

Linked Data

dbSNP Id: rs12644427

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122862232A>G , CM000666.2:g.122862232A>G GRCh38
NC_000004.11:g.123783387A>G , CM000666.1:g.123783387A>G GRCh37
NC_000004.10:g.124002837A>G NCBI36
NG_029067.1:g.40525A>G
NG_029067.2:g.40525A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264498.9:c.578-14089A>G ENSP00000264498.4:n.578-14089A>G
ENST00000264498.8:c.578-14089A>G ENSP00000264498.4:n.578-14089A>G
ENST00000644866.2:c.179-14089A>G MANE Select ENSP00000494222.1:n.179-14089A>G
ENST00000264498.7:c.578-14089A>G ENSP00000264498.3:n.578-14089A>G
ENST00000608478.1:c.179-14089A>G ENSP00000477134.1:n.179-14089A>G
ENST00000614010.4:c.578-14089A>G ENSP00000478620.1:n.578-14089A>G
NM_002006.4:c.578-14089A>G NP_001997.5:n.578-14089A>G
NM_001361665.1:c.179-14089A>G NP_001348594.1:n.179-14089A>G
NM_002006.5:c.578-14089A>G NP_001997.5:n.578-14089A>G
NM_001361665.2:c.179-14089A>G MANE Select NP_001348594.1:n.179-14089A>G
NM_002006.6:c.578-14089A>G NP_001997.5:n.578-14089A>G