Canonical Allele Identifier: CA2672442395
Gene: FGA HGNC NCBI

Linked Data

gnomAD v4: 4-154583797-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154583797G>T , CM000666.2:g.154583797G>T GRCh38
NC_000004.11:g.155504949G>T , CM000666.1:g.155504949G>T GRCh37
NC_000004.10:g.155724399G>T NCBI36
NG_008832.1:g.11949C>A , LRG_557:g.11949C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651975.2:c.*327C>A ENSP00000498441.1:n.*327C>A
ENST00000651975.1:c.*327C>A ENSP00000498441.1:n.*327C>A
ENST00000302053.7:c.*327C>A ENSP00000306361.3:n.*327C>A
NM_000508.3:c.*327C>A , LRG_557t1:c.*327C>A NP_000499.1:n.*327C>A
NM_000508.4:c.*327C>A NP_000499.1:n.*327C>A
NM_000508.5:c.*327C>A NP_000499.1:n.*327C>A
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