Canonical Allele Identifier: CA105260890

Gene: FGF2

Linked Data

• dbSNP Id: rs567321561
• gnomAD v3: 4-122851498-T-C
• gnomAD v4: 4-122851498-T-C
• MyVariant Identifiers: chr4:g.123772653T>C (hg19) ; chr4:g.122851498T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122851498T>C , CM000666.2:g.122851498T>C	GRCh38
NC_000004.11:g.123772653T>C , CM000666.1:g.123772653T>C	GRCh37
NC_000004.10:g.123992103T>C	NCBI36
NG_029067.1:g.29791T>C
NG_029067.2:g.29791T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264498.9:c.577+24146T>C	ENSP00000264498.4:n.577+24146T>C
ENST00000264498.8:c.577+24146T>C	ENSP00000264498.4:n.577+24146T>C
ENST00000644866.2:c.178+24146T>C MANE Select	ENSP00000494222.1:n.178+24146T>C
ENST00000264498.7:c.577+24146T>C	ENSP00000264498.3:n.577+24146T>C
ENST00000608478.1:c.178+24146T>C	ENSP00000477134.1:n.178+24146T>C
ENST00000614010.4:c.577+24146T>C	ENSP00000478620.1:n.577+24146T>C
NM_002006.4:c.577+24146T>C	NP_001997.5:n.577+24146T>C
NM_001361665.1:c.178+24146T>C	NP_001348594.1:n.178+24146T>C
NM_002006.5:c.577+24146T>C	NP_001997.5:n.577+24146T>C
NM_001361665.2:c.178+24146T>C MANE Select	NP_001348594.1:n.178+24146T>C
NM_002006.6:c.577+24146T>C	NP_001997.5:n.577+24146T>C