Canonical Allele Identifier: CA2672442428
Gene: FGA HGNC NCBI

Linked Data

gnomAD v4: 4-154583826-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154583826C>G , CM000666.2:g.154583826C>G GRCh38
NC_000004.11:g.155504978C>G , CM000666.1:g.155504978C>G GRCh37
NC_000004.10:g.155724428C>G NCBI36
NG_008832.1:g.11920G>C , LRG_557:g.11920G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651975.2:c.*298G>C ENSP00000498441.1:n.*298G>C
ENST00000651975.1:c.*298G>C ENSP00000498441.1:n.*298G>C
ENST00000302053.7:c.*298G>C ENSP00000306361.3:n.*298G>C
NM_000508.3:c.*298G>C , LRG_557t1:c.*298G>C NP_000499.1:n.*298G>C
NM_000508.4:c.*298G>C NP_000499.1:n.*298G>C
NM_000508.5:c.*298G>C NP_000499.1:n.*298G>C
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