Canonical Allele Identifier: CA1846866285

Gene: GRHPR

Linked Data

• dbSNP Id: rs2736664
• gnomAD v4: 9-37426527-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37426527C>G , CM000671.2:g.37426527C>G	GRCh38
NC_000009.11:g.37426524C>G , CM000671.1:g.37426524C>G	GRCh37
NC_000009.10:g.37416524C>G	NCBI36
NG_008135.1:g.8818C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.288-11C>G MANE Select	ENSP00000313432.6:n.288-11C>G
ENST00000318158.10:c.288-11C>G	ENSP00000313432.6:n.288-11C>G
ENST00000377824.8:n.325-11C>G
ENST00000460882.5:n.315-11C>G
ENST00000487399.5:n.829C>G
ENST00000491488.5:n.110-1957C>G
ENST00000493368.5:n.345-11C>G
ENST00000607784.1:c.288-11C>G	ENSP00000475569.1:n.288-11C>G
NM_012203.1:c.288-11C>G	NP_036335.1:n.288-11C>G
XM_005251631.1:c.84-1957C>G	XP_005251688.1:n.84-1957C>G
XM_011518073.1:c.-475-11C>G	XP_011516375.1:n.-475-11C>G
XR_929374.1:n.373-11C>G
XM_017015320.2:c.288-11C>G	XP_016870809.1:n.288-11C>G
XM_017015321.2:c.288-11C>G	XP_016870810.1:n.288-11C>G
XM_017015323.2:c.-475-11C>G	XP_016870812.1:n.-475-11C>G
XM_024447716.1:c.561-11C>G	XP_024303484.1:n.561-11C>G
XM_024447717.1:c.561-11C>G	XP_024303485.1:n.561-11C>G
XR_002956828.1:n.576-11C>G
XR_002956829.1:n.576-11C>G
XR_002956830.1:n.347-11C>G
XR_002956831.1:n.139-1957C>G
XR_002956832.1:n.347-11C>G
NM_012203.2:c.288-11C>G MANE Select	NP_036335.1:n.288-11C>G