Canonical Allele Identifier: CA358533872

Gene: FGA

Linked Data

• ClinVar Variation Id: 16401
• ClinVar RCV Id: RCV000017842
• dbSNP Id: rs1403508334
• MyVariant Identifiers: chr4:g.155510655C>G (hg19) ; chr4:g.154589503C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589503C>G , CM000666.2:g.154589503C>G	GRCh38
NC_000004.11:g.155510655C>G , CM000666.1:g.155510655C>G	GRCh37
NC_000004.10:g.155730105C>G	NCBI36
NG_008832.1:g.6243G>C , LRG_557:g.6243G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.114G>C	ENSP00000498441.1:p.Arg38Ser
ENST00000403106.8:c.114G>C MANE Select	ENSP00000385981.3:p.Arg38Ser
ENST00000651975.1:c.114G>C	ENSP00000498441.1:p.Arg38Ser
ENST00000302053.7:c.114G>C	ENSP00000306361.3:p.Arg38Ser
ENST00000403106.7:c.114G>C	ENSP00000385981.3:p.Arg38Ser
ENST00000622532.1:c.114G>C	ENSP00000478487.1:p.Arg38Ser
NM_000508.3:c.114G>C , LRG_557t1:c.114G>C	NP_000499.1:p.Arg38Ser
NM_021871.2:c.114G>C , LRG_557t2:c.114G>C	NP_068657.1:p.Arg38Ser
NM_000508.4:c.114G>C	NP_000499.1:p.Arg38Ser
NM_021871.3:c.114G>C	NP_068657.1:p.Arg38Ser
NM_021871.4:c.114G>C MANE Select	NP_068657.1:p.Arg38Ser
NM_000508.5:c.114G>C	NP_000499.1:p.Arg38Ser