Canonical Allele Identifier: CA441376830

Gene: FGF2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122826931C>G , CM000666.2:g.122826931C>G	GRCh38
NC_000004.11:g.123748086C>G , CM000666.1:g.123748086C>G	GRCh37
NC_000004.10:g.123967536C>G	NCBI36
NG_029067.1:g.5224C>G
NG_029067.2:g.5224C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264498.9:c.156C>G	ENSP00000264498.4:p.Ser52=
ENST00000264498.8:c.156C>G	ENSP00000264498.4:p.Ser52=
ENST00000644866.2:c.-244C>G MANE Select	ENSP00000494222.1:n.-244C>G
ENST00000264498.7:c.156C>G	ENSP00000264498.3:p.Ser52=
ENST00000608478.1:c.-244C>G	ENSP00000477134.1:n.-244C>G
ENST00000614010.4:c.156C>G	ENSP00000478620.1:p.Ser52=
NM_002006.4:c.156C>G	NP_001997.5:p.Ser52=
NM_001361665.1:c.-244C>G	NP_001348594.1:n.-244C>G
NM_002006.5:c.156C>G	NP_001997.5:p.Ser52=
NM_001361665.2:c.-244C>G MANE Select	NP_001348594.1:n.-244C>G
NM_002006.6:c.156C>G	NP_001997.5:p.Ser52=