Canonical Allele Identifier: CA192896122

Gene: GRHPR

Linked Data

• dbSNP Id: rs890726175
• gnomAD v4: 9-37436595-A-G
• MyVariant Identifiers: chr9:g.37436592A>G (hg19) ; chr9:g.37436595A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436595A>G , CM000671.2:g.37436595A>G	GRCh38
NC_000009.11:g.37436592A>G , CM000671.1:g.37436592A>G	GRCh37
NC_000009.10:g.37426592A>G	NCBI36
NG_008135.1:g.18886A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-66A>G MANE Select	ENSP00000313432.6:n.866-66A>G
ENST00000318158.10:c.866-66A>G	ENSP00000313432.6:n.866-66A>G
ENST00000460882.5:n.893-66A>G
ENST00000480596.5:n.1567-66A>G
ENST00000491488.5:n.571-66A>G
ENST00000494290.1:c.*52-286A>G	ENSP00000432021.1:n.*52-286A>G
ENST00000497693.1:n.4434-66A>G
NM_012203.1:c.866-66A>G	NP_036335.1:n.866-66A>G
XM_005251631.1:c.545-66A>G	XP_005251688.1:n.545-66A>G
XM_011518073.1:c.464-66A>G	XP_011516375.1:n.464-66A>G
XM_017015320.2:c.946-816A>G	XP_016870809.1:n.946-816A>G
XM_017015321.2:c.866-816A>G	XP_016870810.1:n.866-816A>G
XM_017015323.2:c.544-816A>G	XP_016870812.1:n.544-816A>G
XM_024447716.1:c.1219-816A>G	XP_024303484.1:n.1219-816A>G
XM_024447717.1:c.1139-816A>G	XP_024303485.1:n.1139-816A>G
XR_002956828.1:n.1234-816A>G
XR_002956829.1:n.1154-816A>G
XR_002956830.1:n.2286-66A>G
XR_002956831.1:n.1961-66A>G
XR_002956832.1:n.1285-66A>G
NM_012203.2:c.866-66A>G MANE Select	NP_036335.1:n.866-66A>G