Canonical Allele Identifier: CA3114940

Gene: FGA

Linked Data

• ClinVar Variation Id: 523628
• ClinVar RCV Id: RCV000627058 ; RCV004527690
• dbSNP Id: rs771023837
• ExAC: 4:155505788 C / T
• gnomAD v2: 4-155505788-C-T
• gnomAD v3: 4-154584636-C-T
• gnomAD v4: 4-154584636-C-T
• COSMIC: COSM265803
• MyVariant Identifiers: chr4:g.155505788C>T (hg19) ; chr4:g.154584636C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154584636C>T , CM000666.2:g.154584636C>T	GRCh38
NC_000004.11:g.155505788C>T , CM000666.1:g.155505788C>T	GRCh37
NC_000004.10:g.155725238C>T	NCBI36
NG_008832.1:g.11110G>A , LRG_557:g.11110G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651975.2:c.2089G>A	ENSP00000498441.1:p.Gly697Ser
ENST00000651975.1:c.2089G>A	ENSP00000498441.1:p.Gly697Ser
ENST00000302053.7:c.2089G>A	ENSP00000306361.3:p.Gly697Ser
NM_000508.3:c.2089G>A , LRG_557t1:c.2089G>A	NP_000499.1:p.Gly697Ser
NM_000508.4:c.2089G>A	NP_000499.1:p.Gly697Ser
NM_000508.5:c.2089G>A	NP_000499.1:p.Gly697Ser