Canonical Allele Identifier: CA587805448

Gene: GRHPR

Linked Data

• dbSNP Id: rs1268925188
• gnomAD v2: 9-37436626-T-A
• gnomAD v3: 9-37436629-T-A
• gnomAD v4: 9-37436629-T-A
• MyVariant Identifiers: chr9:g.37436626T>A (hg19) ; chr9:g.37436629T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436629T>A , CM000671.2:g.37436629T>A	GRCh38
NC_000009.11:g.37436626T>A , CM000671.1:g.37436626T>A	GRCh37
NC_000009.10:g.37426626T>A	NCBI36
NG_008135.1:g.18920T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-32T>A MANE Select	ENSP00000313432.6:n.866-32T>A
ENST00000318158.10:c.866-32T>A	ENSP00000313432.6:n.866-32T>A
ENST00000460882.5:n.893-32T>A
ENST00000480596.5:n.1567-32T>A
ENST00000491488.5:n.571-32T>A
ENST00000494290.1:c.*52-252T>A	ENSP00000432021.1:n.*52-252T>A
ENST00000497693.1:n.4434-32T>A
NM_012203.1:c.866-32T>A	NP_036335.1:n.866-32T>A
XM_005251631.1:c.545-32T>A	XP_005251688.1:n.545-32T>A
XM_011518073.1:c.464-32T>A	XP_011516375.1:n.464-32T>A
XM_017015320.2:c.946-782T>A	XP_016870809.1:n.946-782T>A
XM_017015321.2:c.866-782T>A	XP_016870810.1:n.866-782T>A
XM_017015323.2:c.544-782T>A	XP_016870812.1:n.544-782T>A
XM_024447716.1:c.1219-782T>A	XP_024303484.1:n.1219-782T>A
XM_024447717.1:c.1139-782T>A	XP_024303485.1:n.1139-782T>A
XR_002956828.1:n.1234-782T>A
XR_002956829.1:n.1154-782T>A
XR_002956830.1:n.2286-32T>A
XR_002956831.1:n.1961-32T>A
XR_002956832.1:n.1285-32T>A
NM_012203.2:c.866-32T>A MANE Select	NP_036335.1:n.866-32T>A