Canonical Allele Identifier: CA2672442415
Gene: FGA HGNC NCBI

Linked Data

gnomAD v4: 4-154583814-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154583814A>T , CM000666.2:g.154583814A>T GRCh38
NC_000004.11:g.155504966A>T , CM000666.1:g.155504966A>T GRCh37
NC_000004.10:g.155724416A>T NCBI36
NG_008832.1:g.11932T>A , LRG_557:g.11932T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651975.2:c.*310T>A ENSP00000498441.1:n.*310T>A
ENST00000651975.1:c.*310T>A ENSP00000498441.1:n.*310T>A
ENST00000302053.7:c.*310T>A ENSP00000306361.3:n.*310T>A
NM_000508.3:c.*310T>A , LRG_557t1:c.*310T>A NP_000499.1:n.*310T>A
NM_000508.4:c.*310T>A NP_000499.1:n.*310T>A
NM_000508.5:c.*310T>A NP_000499.1:n.*310T>A
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