Canonical Allele Identifier: CA2686820369
Gene: GSR HGNC NCBI

Linked Data

gnomAD v4: 8-30727997-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.30727997T>A , CM000670.2:g.30727997T>A GRCh38
NC_000008.10:g.30585514T>A , CM000670.1:g.30585514T>A GRCh37
NC_000008.9:g.30705056T>A NCBI36
NG_027719.1:g.4973A>T

Transcript Alleles

HGVS Amino-acid Change
NM_000637.4:c.-162A>T NP_000628.2:n.-162A>T
NM_001195102.2:c.-162A>T NP_001182031.1:n.-162A>T
NM_001195103.2:c.-162A>T NP_001182032.1:n.-162A>T
NM_001195104.2:c.-162A>T NP_001182033.1:n.-162A>T
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