Canonical Allele Identifier: CA174826642

Gene: GSR

Linked Data

• dbSNP Id: rs949203700
• gnomAD v2: 8-30585479-C-T
• gnomAD v3: 8-30727962-C-T
• gnomAD v4: 8-30727962-C-T
• MyVariant Identifiers: chr8:g.30585479C>T (hg19) ; chr8:g.30727962C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.30727962C>T , CM000670.2:g.30727962C>T	GRCh38
NC_000008.10:g.30585479C>T , CM000670.1:g.30585479C>T	GRCh37
NC_000008.9:g.30705021C>T	NCBI36
NG_027719.1:g.5008G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000637.3:c.-127G>A	NP_000628.2:n.-127G>A
NM_001195102.1:c.-127G>A	NP_001182031.1:n.-127G>A
NM_001195103.1:c.-127G>A	NP_001182032.1:n.-127G>A
NM_001195104.1:c.-127G>A	NP_001182033.1:n.-127G>A
NM_000637.4:c.-127G>A	NP_000628.2:n.-127G>A
NM_001195102.2:c.-127G>A	NP_001182031.1:n.-127G>A
NM_001195103.2:c.-127G>A	NP_001182032.1:n.-127G>A
NM_001195104.2:c.-127G>A	NP_001182033.1:n.-127G>A