Canonical Allele Identifier: CA358526707

Gene: FGA

Linked Data

• dbSNP Id: rs1306146396
• gnomAD v2: 4-155506849-T-G
• gnomAD v4: 4-154585697-T-G
• MyVariant Identifiers: chr4:g.155506849T>G (hg19) ; chr4:g.154585697T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154585697T>G , CM000666.2:g.154585697T>G	GRCh38
NC_000004.11:g.155506849T>G , CM000666.1:g.155506849T>G	GRCh37
NC_000004.10:g.155726299T>G	NCBI36
NG_008832.1:g.10049A>C , LRG_557:g.10049A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.1732A>C	ENSP00000498441.1:p.Ser578Arg
ENST00000403106.8:c.1732A>C MANE Select	ENSP00000385981.3:p.Ser578Arg
ENST00000651975.1:c.1732A>C	ENSP00000498441.1:p.Ser578Arg
ENST00000302053.7:c.1732A>C	ENSP00000306361.3:p.Ser578Arg
ENST00000403106.7:c.1732A>C	ENSP00000385981.3:p.Ser578Arg
ENST00000622532.1:c.657A>C	ENSP00000478487.1:p.Gln219His
NM_000508.3:c.1732A>C , LRG_557t1:c.1732A>C	NP_000499.1:p.Ser578Arg
NM_021871.2:c.1732A>C , LRG_557t2:c.1732A>C	NP_068657.1:p.Ser578Arg
NM_000508.4:c.1732A>C	NP_000499.1:p.Ser578Arg
NM_021871.3:c.1732A>C	NP_068657.1:p.Ser578Arg
NM_021871.4:c.1732A>C MANE Select	NP_068657.1:p.Ser578Arg
NM_000508.5:c.1732A>C	NP_000499.1:p.Ser578Arg