Canonical Allele Identifier: CA2672442427

Gene: FGA

Linked Data

• gnomAD v4: 4-154583824-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154583824T>C , CM000666.2:g.154583824T>C	GRCh38
NC_000004.11:g.155504976T>C , CM000666.1:g.155504976T>C	GRCh37
NC_000004.10:g.155724426T>C	NCBI36
NG_008832.1:g.11922A>G , LRG_557:g.11922A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.*300A>G	ENSP00000498441.1:n.*300A>G
ENST00000651975.1:c.*300A>G	ENSP00000498441.1:n.*300A>G
ENST00000302053.7:c.*300A>G	ENSP00000306361.3:n.*300A>G
NM_000508.3:c.*300A>G , LRG_557t1:c.*300A>G	NP_000499.1:n.*300A>G
NM_000508.4:c.*300A>G	NP_000499.1:n.*300A>G
NM_000508.5:c.*300A>G	NP_000499.1:n.*300A>G