Canonical Allele Identifier: CA174826644
Gene: GSR HGNC NCBI

Linked Data

dbSNP Id: rs1030557802
MyVariant Identifiers: chr8:g.30585491C>G (hg19) chr8:g.30727974C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.30727974C>G , CM000670.2:g.30727974C>G GRCh38
NC_000008.10:g.30585491C>G , CM000670.1:g.30585491C>G GRCh37
NC_000008.9:g.30705033C>G NCBI36
NG_027719.1:g.4996G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000637.4:c.-139G>C NP_000628.2:n.-139G>C
NM_001195102.2:c.-139G>C NP_001182031.1:n.-139G>C
NM_001195103.2:c.-139G>C NP_001182032.1:n.-139G>C
NM_001195104.2:c.-139G>C NP_001182033.1:n.-139G>C
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