Canonical Allele Identifier: CA126479
Gene: FGA HGNC NCBI

Linked Data

ClinVar Variation Id: 16405
ClinVar RCV Id: RCV000017865 RCV001508522
dbSNP Id: rs121909610
MyVariant Identifiers: chr4:g.155507223C>T (hg19) chr4:g.154586071C>T (hg38)
PubMed: PMID:1675636
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154586071C>T , CM000666.2:g.154586071C>T GRCh38
NC_000004.11:g.155507223C>T , CM000666.1:g.155507223C>T GRCh37
NC_000004.10:g.155726673C>T NCBI36
NG_008832.1:g.9675G>A , LRG_557:g.9675G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651975.2:c.1358G>A ENSP00000498441.1:p.Ser453Asn
ENST00000403106.8:c.1358G>A MANE Select ENSP00000385981.3:p.Ser453Asn
ENST00000651975.1:c.1358G>A ENSP00000498441.1:p.Ser453Asn
ENST00000302053.7:c.1358G>A ENSP00000306361.3:p.Ser453Asn
ENST00000403106.7:c.1358G>A ENSP00000385981.3:p.Ser453Asn
ENST00000622532.1:c.644-361G>A ENSP00000478487.1:n.644-361G>A
NM_000508.3:c.1358G>A , LRG_557t1:c.1358G>A NP_000499.1:p.Ser453Asn
NM_021871.2:c.1358G>A , LRG_557t2:c.1358G>A NP_068657.1:p.Ser453Asn
NM_000508.4:c.1358G>A NP_000499.1:p.Ser453Asn
NM_021871.3:c.1358G>A NP_068657.1:p.Ser453Asn
NM_021871.4:c.1358G>A MANE Select NP_068657.1:p.Ser453Asn
NM_000508.5:c.1358G>A NP_000499.1:p.Ser453Asn
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