Canonical Allele Identifier: CA358533865

Gene: FGA

Linked Data

• dbSNP Id: rs121909614
• gnomAD v3: 4-154589501-A-G
• gnomAD v4: 4-154589501-A-G
• MyVariant Identifiers: chr4:g.155510653A>G (hg19) ; chr4:g.154589501A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589501A>G , CM000666.2:g.154589501A>G	GRCh38
NC_000004.11:g.155510653A>G , CM000666.1:g.155510653A>G	GRCh37
NC_000004.10:g.155730103A>G	NCBI36
NG_008832.1:g.6245T>C , LRG_557:g.6245T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.116T>C	ENSP00000498441.1:p.Val39Ala
ENST00000403106.8:c.116T>C MANE Select	ENSP00000385981.3:p.Val39Ala
ENST00000651975.1:c.116T>C	ENSP00000498441.1:p.Val39Ala
ENST00000302053.7:c.116T>C	ENSP00000306361.3:p.Val39Ala
ENST00000403106.7:c.116T>C	ENSP00000385981.3:p.Val39Ala
ENST00000622532.1:c.116T>C	ENSP00000478487.1:p.Val39Ala
NM_000508.3:c.116T>C , LRG_557t1:c.116T>C	NP_000499.1:p.Val39Ala
NM_021871.2:c.116T>C , LRG_557t2:c.116T>C	NP_068657.1:p.Val39Ala
NM_000508.4:c.116T>C	NP_000499.1:p.Val39Ala
NM_021871.3:c.116T>C	NP_068657.1:p.Val39Ala
NM_021871.4:c.116T>C MANE Select	NP_068657.1:p.Val39Ala
NM_000508.5:c.116T>C	NP_000499.1:p.Val39Ala