Canonical Allele Identifier: CA2689952210
Gene: GRHPR HGNC NCBI

Linked Data

gnomAD v4: 9-37422695-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37422695T>C , CM000671.2:g.37422695T>C GRCh38
NC_000009.11:g.37422692T>C , CM000671.1:g.37422692T>C GRCh37
NC_000009.10:g.37412692T>C NCBI36
NG_008135.1:g.4986T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.10:c.-56T>C ENSP00000313432.6:n.-56T>C
ENST00000493368.5:n.30T>C
XR_929374.1:n.30T>C
XM_017015320.2:c.-56T>C XP_016870809.1:n.-56T>C
XM_017015321.2:c.-56T>C XP_016870810.1:n.-56T>C
XM_017015323.2:c.-818T>C XP_016870812.1:n.-818T>C
XM_024447716.1:c.246T>C XP_024303484.1:p.Ala82=
XM_024447717.1:c.246T>C XP_024303485.1:p.Ala82=
XR_002956828.1:n.261T>C
XR_002956829.1:n.261T>C
XR_002956830.1:n.4T>C
XR_002956832.1:n.4T>C
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