Canonical Allele Identifier: CA3115402

Gene: FGA

Linked Data

• dbSNP Id: rs368266292
• ExAC: 4:155510736 C / T
• gnomAD v2: 4-155510736-C-T
• gnomAD v3: 4-154589584-C-T
• gnomAD v4: 4-154589584-C-T
• MyVariant Identifiers: chr4:g.155510736C>T (hg19) ; chr4:g.154589584C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589584C>T , CM000666.2:g.154589584C>T	GRCh38
NC_000004.11:g.155510736C>T , CM000666.1:g.155510736C>T	GRCh37
NC_000004.10:g.155730186C>T	NCBI36
NG_008832.1:g.6162G>A , LRG_557:g.6162G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651975.2:c.55-22G>A	ENSP00000498441.1:n.55-22G>A
ENST00000403106.8:c.55-22G>A MANE Select	ENSP00000385981.3:n.55-22G>A
ENST00000651975.1:c.55-22G>A	ENSP00000498441.1:n.55-22G>A
ENST00000302053.7:c.55-22G>A	ENSP00000306361.3:n.55-22G>A
ENST00000403106.7:c.55-22G>A	ENSP00000385981.3:n.55-22G>A
ENST00000622532.1:c.55-22G>A	ENSP00000478487.1:n.55-22G>A
NM_000508.3:c.55-22G>A , LRG_557t1:c.55-22G>A	NP_000499.1:n.55-22G>A
NM_021871.2:c.55-22G>A , LRG_557t2:c.55-22G>A	NP_068657.1:n.55-22G>A
NM_000508.4:c.55-22G>A	NP_000499.1:n.55-22G>A
NM_021871.3:c.55-22G>A	NP_068657.1:n.55-22G>A
NM_021871.4:c.55-22G>A MANE Select	NP_068657.1:n.55-22G>A
NM_000508.5:c.55-22G>A	NP_000499.1:n.55-22G>A