Canonical Allele Identifier: CA465004011

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37428568-C-A
• MyVariant Identifiers: chr9:g.37428565C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428568C>A , CM000671.2:g.37428568C>A	GRCh38
NC_000009.11:g.37428565C>A , CM000671.1:g.37428565C>A	GRCh37
NC_000009.10:g.37418565C>A	NCBI36
NG_008135.1:g.10859C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.489C>A MANE Select	ENSP00000313432.6:p.Arg163=
ENST00000318158.10:c.489C>A	ENSP00000313432.6:p.Arg163=
ENST00000377824.8:n.526C>A
ENST00000460882.5:n.516C>A
ENST00000480596.5:n.31C>A
ENST00000491488.5:n.194C>A
ENST00000493368.5:n.546C>A
ENST00000497693.1:n.863C>A
ENST00000607784.1:c.489C>A	ENSP00000475569.1:p.Arg163=
NM_012203.1:c.489C>A	NP_036335.1:p.Arg163=
XM_005251631.1:c.168C>A	XP_005251688.1:p.Arg56=
XM_011518073.1:c.-274C>A	XP_011516375.1:n.-274C>A
XR_929374.1:n.574C>A
XM_017015320.2:c.489C>A	XP_016870809.1:p.Arg163=
XM_017015321.2:c.489C>A	XP_016870810.1:p.Arg163=
XM_017015323.2:c.-274C>A	XP_016870812.1:n.-274C>A
XM_024447716.1:c.762C>A	XP_024303484.1:p.Arg254=
XM_024447717.1:c.762C>A	XP_024303485.1:p.Arg254=
XR_002956828.1:n.777C>A
XR_002956829.1:n.777C>A
XR_002956830.1:n.548C>A
XR_002956831.1:n.223C>A
XR_002956832.1:n.548C>A
NM_012203.2:c.489C>A MANE Select	NP_036335.1:p.Arg163=