Canonical Allele Identifier: CA192885732

Gene: GRHPR

Linked Data

• dbSNP Id: rs1046879824
• MyVariant Identifiers: chr9:g.37422692T>G (hg19) ; chr9:g.37422695T>G (hg38)

Genomic Alleles

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

Transcript Alleles

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