Canonical Allele Identifier: CA2672442406

Gene: FGA

Linked Data

• gnomAD v4: 4-154583805-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154583805A>C , CM000666.2:g.154583805A>C	GRCh38
NC_000004.11:g.155504957A>C , CM000666.1:g.155504957A>C	GRCh37
NC_000004.10:g.155724407A>C	NCBI36
NG_008832.1:g.11941T>G , LRG_557:g.11941T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.*319T>G	ENSP00000498441.1:n.*319T>G
ENST00000651975.1:c.*319T>G	ENSP00000498441.1:n.*319T>G
ENST00000302053.7:c.*319T>G	ENSP00000306361.3:n.*319T>G
NM_000508.3:c.*319T>G , LRG_557t1:c.*319T>G	NP_000499.1:n.*319T>G
NM_000508.4:c.*319T>G	NP_000499.1:n.*319T>G
NM_000508.5:c.*319T>G	NP_000499.1:n.*319T>G