Canonical Allele Identifier: CA3115043

Gene: FGA

Linked Data

• dbSNP Id: rs750277272
• ExAC: 4:155506851 G / C
• gnomAD v2: 4-155506851-G-C
• gnomAD v4: 4-154585699-G-C
• MyVariant Identifiers: chr4:g.155506851G>C (hg19) ; chr4:g.154585699G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154585699G>C , CM000666.2:g.154585699G>C	GRCh38
NC_000004.11:g.155506851G>C , CM000666.1:g.155506851G>C	GRCh37
NC_000004.10:g.155726301G>C	NCBI36
NG_008832.1:g.10047C>G , LRG_557:g.10047C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.1730C>G	ENSP00000498441.1:p.Ser577Ter
ENST00000403106.8:c.1730C>G MANE Select	ENSP00000385981.3:p.Ser577Ter
ENST00000651975.1:c.1730C>G	ENSP00000498441.1:p.Ser577Ter
ENST00000302053.7:c.1730C>G	ENSP00000306361.3:p.Ser577Ter
ENST00000403106.7:c.1730C>G	ENSP00000385981.3:p.Ser577Ter
ENST00000622532.1:c.655C>G	ENSP00000478487.1:p.Gln219Glu
NM_000508.3:c.1730C>G , LRG_557t1:c.1730C>G	NP_000499.1:p.Ser577Ter
NM_021871.2:c.1730C>G , LRG_557t2:c.1730C>G	NP_068657.1:p.Ser577Ter
NM_000508.4:c.1730C>G	NP_000499.1:p.Ser577Ter
NM_021871.3:c.1730C>G	NP_068657.1:p.Ser577Ter
NM_021871.4:c.1730C>G MANE Select	NP_068657.1:p.Ser577Ter
NM_000508.5:c.1730C>G	NP_000499.1:p.Ser577Ter