Canonical Allele Identifier: CA15323047

Gene: FGF2

Linked Data

• dbSNP Id: rs308379
• gnomAD v2: 4-123782896-A-T
• gnomAD v3: 4-122861741-A-T
• gnomAD v4: 4-122861741-A-T
• MyVariant Identifiers: chr4:g.123782896A>T (hg19) ; chr4:g.122861741A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122861741A>T , CM000666.2:g.122861741A>T	GRCh38
NC_000004.11:g.123782896A>T , CM000666.1:g.123782896A>T	GRCh37
NC_000004.10:g.124002346A>T	NCBI36
NG_029067.1:g.40034A>T
NG_029067.2:g.40034A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264498.9:c.578-14580A>T	ENSP00000264498.4:n.578-14580A>T
ENST00000264498.8:c.578-14580A>T	ENSP00000264498.4:n.578-14580A>T
ENST00000644866.2:c.179-14580A>T MANE Select	ENSP00000494222.1:n.179-14580A>T
ENST00000264498.7:c.578-14580A>T	ENSP00000264498.3:n.578-14580A>T
ENST00000608478.1:c.179-14580A>T	ENSP00000477134.1:n.179-14580A>T
ENST00000614010.4:c.578-14580A>T	ENSP00000478620.1:n.578-14580A>T
NM_002006.4:c.578-14580A>T	NP_001997.5:n.578-14580A>T
NM_001361665.1:c.179-14580A>T	NP_001348594.1:n.179-14580A>T
NM_002006.5:c.578-14580A>T	NP_001997.5:n.578-14580A>T
NM_001361665.2:c.179-14580A>T MANE Select	NP_001348594.1:n.179-14580A>T
NM_002006.6:c.578-14580A>T	NP_001997.5:n.578-14580A>T