Canonical Allele Identifier: CA2689953197

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37426440-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37426440T>G , CM000671.2:g.37426440T>G	GRCh38
NC_000009.11:g.37426437T>G , CM000671.1:g.37426437T>G	GRCh37
NC_000009.10:g.37416437T>G	NCBI36
NG_008135.1:g.8731T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.288-98T>G MANE Select	ENSP00000313432.6:n.288-98T>G
ENST00000318158.10:c.288-98T>G	ENSP00000313432.6:n.288-98T>G
ENST00000377824.8:n.325-98T>G
ENST00000460882.5:n.315-98T>G
ENST00000487399.5:n.742T>G
ENST00000491488.5:n.110-2044T>G
ENST00000493368.5:n.345-98T>G
ENST00000607784.1:c.288-98T>G	ENSP00000475569.1:n.288-98T>G
NM_012203.1:c.288-98T>G	NP_036335.1:n.288-98T>G
XM_005251631.1:c.84-2044T>G	XP_005251688.1:n.84-2044T>G
XM_011518073.1:c.-475-98T>G	XP_011516375.1:n.-475-98T>G
XR_929374.1:n.373-98T>G
XM_017015320.2:c.288-98T>G	XP_016870809.1:n.288-98T>G
XM_017015321.2:c.288-98T>G	XP_016870810.1:n.288-98T>G
XM_017015323.2:c.-475-98T>G	XP_016870812.1:n.-475-98T>G
XM_024447716.1:c.561-98T>G	XP_024303484.1:n.561-98T>G
XM_024447717.1:c.561-98T>G	XP_024303485.1:n.561-98T>G
XR_002956828.1:n.576-98T>G
XR_002956829.1:n.576-98T>G
XR_002956830.1:n.347-98T>G
XR_002956831.1:n.139-2044T>G
XR_002956832.1:n.347-98T>G
NM_012203.2:c.288-98T>G MANE Select	NP_036335.1:n.288-98T>G