Canonical Allele Identifier: CA2672442408
Gene: FGA HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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