Canonical Allele Identifier: CA1067519469

Gene: FGF2

Linked Data

• dbSNP Id: rs1726245801
• gnomAD v3: 4-122852189-T-C
• gnomAD v4: 4-122852189-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122852189T>C , CM000666.2:g.122852189T>C	GRCh38
NC_000004.11:g.123773344T>C , CM000666.1:g.123773344T>C	GRCh37
NC_000004.10:g.123992794T>C	NCBI36
NG_029067.1:g.30482T>C
NG_029067.2:g.30482T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264498.9:c.578-24132T>C	ENSP00000264498.4:n.578-24132T>C
ENST00000264498.8:c.578-24132T>C	ENSP00000264498.4:n.578-24132T>C
ENST00000644866.2:c.179-24132T>C MANE Select	ENSP00000494222.1:n.179-24132T>C
ENST00000264498.7:c.578-24132T>C	ENSP00000264498.3:n.578-24132T>C
ENST00000608478.1:c.179-24132T>C	ENSP00000477134.1:n.179-24132T>C
ENST00000614010.4:c.578-24132T>C	ENSP00000478620.1:n.578-24132T>C
NM_002006.4:c.578-24132T>C	NP_001997.5:n.578-24132T>C
NM_001361665.1:c.179-24132T>C	NP_001348594.1:n.179-24132T>C
NM_002006.5:c.578-24132T>C	NP_001997.5:n.578-24132T>C
NM_001361665.2:c.179-24132T>C MANE Select	NP_001348594.1:n.179-24132T>C
NM_002006.6:c.578-24132T>C	NP_001997.5:n.578-24132T>C