Canonical Allele Identifier: CA1846862742

Gene: GRHPR

Linked Data

• dbSNP Id: rs1822884134
• gnomAD v4: 9-37422698-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37422698A>C , CM000671.2:g.37422698A>C	GRCh38
NC_000009.11:g.37422695A>C , CM000671.1:g.37422695A>C	GRCh37
NC_000009.10:g.37412695A>C	NCBI36
NG_008135.1:g.4989A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.-53A>C MANE Select	ENSP00000313432.6:n.-53A>C
ENST00000318158.10:c.-53A>C	ENSP00000313432.6:n.-53A>C
ENST00000460882.5:n.3A>C
ENST00000493368.5:n.33A>C
XM_005251631.1:c.-53A>C	XP_005251688.1:n.-53A>C
XR_929374.1:n.33A>C
XM_017015320.2:c.-53A>C	XP_016870809.1:n.-53A>C
XM_017015321.2:c.-53A>C	XP_016870810.1:n.-53A>C
XM_017015323.2:c.-815A>C	XP_016870812.1:n.-815A>C
XM_024447716.1:c.249A>C	XP_024303484.1:p.Thr83=
XM_024447717.1:c.249A>C	XP_024303485.1:p.Thr83=
XR_002956828.1:n.264A>C
XR_002956829.1:n.264A>C
XR_002956830.1:n.7A>C
XR_002956831.1:n.3A>C
XR_002956832.1:n.7A>C
NM_012203.2:c.-53A>C MANE Select	NP_036335.1:n.-53A>C