Canonical Allele Identifier: CA2686820352
Gene: GSR HGNC NCBI

Linked Data

gnomAD v4: 8-30727985-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.30727985C>T , CM000670.2:g.30727985C>T GRCh38
NC_000008.10:g.30585502C>T , CM000670.1:g.30585502C>T GRCh37
NC_000008.9:g.30705044C>T NCBI36
NG_027719.1:g.4985G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000637.4:c.-150G>A NP_000628.2:n.-150G>A
NM_001195102.2:c.-150G>A NP_001182031.1:n.-150G>A
NM_001195103.2:c.-150G>A NP_001182032.1:n.-150G>A
NM_001195104.2:c.-150G>A NP_001182033.1:n.-150G>A
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