Canonical Allele Identifier: CA2607936714

Gene: GRHPR

Linked Data

• dbSNP Id: rs1430082256
• gnomAD v4: 9-37436796-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436796A>G , CM000671.2:g.37436796A>G	GRCh38
NC_000009.11:g.37436793A>G , CM000671.1:g.37436793A>G	GRCh37
NC_000009.10:g.37426793A>G	NCBI36
NG_008135.1:g.19087A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*14A>G MANE Select	ENSP00000313432.6:n.*14A>G
ENST00000318158.10:c.*14A>G	ENSP00000313432.6:n.*14A>G
ENST00000460882.5:n.1028A>G
ENST00000480596.5:n.1702A>G
ENST00000494290.1:c.*52-85A>G	ENSP00000432021.1:n.*52-85A>G
ENST00000497693.1:n.4569A>G
NM_012203.1:c.*14A>G	NP_036335.1:n.*14A>G
XM_005251631.1:c.*14A>G	XP_005251688.1:n.*14A>G
XM_011518073.1:c.*14A>G	XP_011516375.1:n.*14A>G
XM_017015320.2:c.946-615A>G	XP_016870809.1:n.946-615A>G
XM_017015321.2:c.866-615A>G	XP_016870810.1:n.866-615A>G
XM_017015323.2:c.544-615A>G	XP_016870812.1:n.544-615A>G
XM_024447716.1:c.1219-615A>G	XP_024303484.1:n.1219-615A>G
XM_024447717.1:c.1139-615A>G	XP_024303485.1:n.1139-615A>G
XR_002956828.1:n.1234-615A>G
XR_002956829.1:n.1154-615A>G
XR_002956830.1:n.2421A>G
XR_002956831.1:n.2096A>G
XR_002956832.1:n.1420A>G
NM_012203.2:c.*14A>G MANE Select	NP_036335.1:n.*14A>G