Canonical Allele Identifier: CA465004086

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37429766-T-C
• MyVariant Identifiers: chr9:g.37429763T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429766T>C , CM000671.2:g.37429766T>C	GRCh38
NC_000009.11:g.37429763T>C , CM000671.1:g.37429763T>C	GRCh37
NC_000009.10:g.37419763T>C	NCBI36
NG_008135.1:g.12057T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.528T>C MANE Select	ENSP00000313432.6:p.Gly176=
ENST00000318158.10:c.528T>C	ENSP00000313432.6:p.Gly176=
ENST00000377824.8:n.565T>C
ENST00000460882.5:n.555T>C
ENST00000480596.5:n.1229T>C
ENST00000491488.5:n.233T>C
ENST00000494290.1:c.99T>C	ENSP00000432021.1:p.Gly33=
ENST00000497693.1:n.2061T>C
ENST00000607784.1:c.528T>C	ENSP00000475569.1:p.Gly176=
NM_012203.1:c.528T>C	NP_036335.1:p.Gly176=
XM_005251631.1:c.207T>C	XP_005251688.1:p.Gly69=
XM_011518073.1:c.126T>C	XP_011516375.1:p.Gly42=
XR_929374.1:n.973T>C
XM_017015320.2:c.528T>C	XP_016870809.1:p.Gly176=
XM_017015321.2:c.528T>C	XP_016870810.1:p.Gly176=
XM_017015323.2:c.126T>C	XP_016870812.1:p.Gly42=
XM_024447716.1:c.801T>C	XP_024303484.1:p.Gly267=
XM_024447717.1:c.801T>C	XP_024303485.1:p.Gly267=
XR_002956828.1:n.816T>C
XR_002956829.1:n.816T>C
XR_002956830.1:n.587T>C
XR_002956831.1:n.262T>C
XR_002956832.1:n.947T>C
NM_012203.2:c.528T>C MANE Select	NP_036335.1:p.Gly176=