Canonical Allele Identifier: CA465006869

Gene: GRHPR

Linked Data

• dbSNP Id: rs1823681219
• MyVariant Identifiers: chr9:g.37436752G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436755G>A , CM000671.2:g.37436755G>A	GRCh38
NC_000009.11:g.37436752G>A , CM000671.1:g.37436752G>A	GRCh37
NC_000009.10:g.37426752G>A	NCBI36
NG_008135.1:g.19046G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.960G>A MANE Select	ENSP00000313432.6:p.Glu320=
ENST00000318158.10:c.960G>A	ENSP00000313432.6:p.Glu320=
ENST00000460882.5:n.987G>A
ENST00000480596.5:n.1661G>A
ENST00000494290.1:c.*52-126G>A	ENSP00000432021.1:n.*52-126G>A
ENST00000497693.1:n.4528G>A
NM_012203.1:c.960G>A	NP_036335.1:p.Glu320=
XM_005251631.1:c.639G>A	XP_005251688.1:p.Glu213=
XM_011518073.1:c.558G>A	XP_011516375.1:p.Glu186=
XM_017015320.2:c.946-656G>A	XP_016870809.1:n.946-656G>A
XM_017015321.2:c.866-656G>A	XP_016870810.1:n.866-656G>A
XM_017015323.2:c.544-656G>A	XP_016870812.1:n.544-656G>A
XM_024447716.1:c.1219-656G>A	XP_024303484.1:n.1219-656G>A
XM_024447717.1:c.1139-656G>A	XP_024303485.1:n.1139-656G>A
XR_002956828.1:n.1234-656G>A
XR_002956829.1:n.1154-656G>A
XR_002956830.1:n.2380G>A
XR_002956831.1:n.2055G>A
XR_002956832.1:n.1379G>A
NM_012203.2:c.960G>A MANE Select	NP_036335.1:p.Glu320=