Canonical Allele Identifier: CA192896327

Gene: GRHPR

Linked Data

• dbSNP Id: rs912026382
• gnomAD v4: 9-37436838-A-G
• MyVariant Identifiers: chr9:g.37436835A>G (hg19) ; chr9:g.37436838A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436838A>G , CM000671.2:g.37436838A>G	GRCh38
NC_000009.11:g.37436835A>G , CM000671.1:g.37436835A>G	GRCh37
NC_000009.10:g.37426835A>G	NCBI36
NG_008135.1:g.19129A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*56A>G MANE Select	ENSP00000313432.6:n.*56A>G
ENST00000318158.10:c.*56A>G	ENSP00000313432.6:n.*56A>G
ENST00000460882.5:n.1070A>G
ENST00000480596.5:n.1744A>G
ENST00000494290.1:c.*52-43A>G	ENSP00000432021.1:n.*52-43A>G
ENST00000497693.1:n.4611A>G
NM_012203.1:c.*56A>G	NP_036335.1:n.*56A>G
XM_005251631.1:c.*56A>G	XP_005251688.1:n.*56A>G
XM_011518073.1:c.*56A>G	XP_011516375.1:n.*56A>G
XM_017015320.2:c.946-573A>G	XP_016870809.1:n.946-573A>G
XM_017015321.2:c.866-573A>G	XP_016870810.1:n.866-573A>G
XM_017015323.2:c.544-573A>G	XP_016870812.1:n.544-573A>G
XM_024447716.1:c.1219-573A>G	XP_024303484.1:n.1219-573A>G
XM_024447717.1:c.1139-573A>G	XP_024303485.1:n.1139-573A>G
XR_002956828.1:n.1234-573A>G
XR_002956829.1:n.1154-573A>G
XR_002956830.1:n.2463A>G
XR_002956831.1:n.2138A>G
XR_002956832.1:n.1462A>G
NM_012203.2:c.*56A>G MANE Select	NP_036335.1:n.*56A>G