Canonical Allele Identifier: CA555606757

Gene: FGA

Linked Data

• dbSNP Id: rs1421891715
• gnomAD v2: 4-155510563-T-C
• gnomAD v4: 4-154589411-T-C
• MyVariant Identifiers: chr4:g.155510563T>C (hg19) ; chr4:g.154589411T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589411T>C , CM000666.2:g.154589411T>C	GRCh38
NC_000004.11:g.155510563T>C , CM000666.1:g.155510563T>C	GRCh37
NC_000004.10:g.155730013T>C	NCBI36
NG_008832.1:g.6335A>G , LRG_557:g.6335A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651975.2:c.180+26A>G	ENSP00000498441.1:n.180+26A>G
ENST00000403106.8:c.180+26A>G MANE Select	ENSP00000385981.3:n.180+26A>G
ENST00000651975.1:c.180+26A>G	ENSP00000498441.1:n.180+26A>G
ENST00000302053.7:c.180+26A>G	ENSP00000306361.3:n.180+26A>G
ENST00000403106.7:c.180+26A>G	ENSP00000385981.3:n.180+26A>G
ENST00000622532.1:c.180+26A>G	ENSP00000478487.1:n.180+26A>G
NM_000508.3:c.180+26A>G , LRG_557t1:c.180+26A>G	NP_000499.1:n.180+26A>G
NM_021871.2:c.180+26A>G , LRG_557t2:c.180+26A>G	NP_068657.1:n.180+26A>G
NM_000508.4:c.180+26A>G	NP_000499.1:n.180+26A>G
NM_021871.3:c.180+26A>G	NP_068657.1:n.180+26A>G
NM_021871.4:c.180+26A>G MANE Select	NP_068657.1:n.180+26A>G
NM_000508.5:c.180+26A>G	NP_000499.1:n.180+26A>G