Canonical Allele Identifier: CA465006819

Gene: GRHPR

Linked Data

• ClinVar Variation Id: 2027854
• ClinVar RCV Id: RCV002866826
• MyVariant Identifiers: chr9:g.37436686C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436689C>T , CM000671.2:g.37436689C>T	GRCh38
NC_000009.11:g.37436686C>T , CM000671.1:g.37436686C>T	GRCh37
NC_000009.10:g.37426686C>T	NCBI36
NG_008135.1:g.18980C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.894C>T MANE Select	ENSP00000313432.6:p.Thr298=
ENST00000318158.10:c.894C>T	ENSP00000313432.6:p.Thr298=
ENST00000460882.5:n.921C>T
ENST00000480596.5:n.1595C>T
ENST00000491488.5:n.599C>T
ENST00000494290.1:c.*52-192C>T	ENSP00000432021.1:n.*52-192C>T
ENST00000497693.1:n.4462C>T
NM_012203.1:c.894C>T	NP_036335.1:p.Thr298=
XM_005251631.1:c.573C>T	XP_005251688.1:p.Thr191=
XM_011518073.1:c.492C>T	XP_011516375.1:p.Thr164=
XM_017015320.2:c.946-722C>T	XP_016870809.1:n.946-722C>T
XM_017015321.2:c.866-722C>T	XP_016870810.1:n.866-722C>T
XM_017015323.2:c.544-722C>T	XP_016870812.1:n.544-722C>T
XM_024447716.1:c.1219-722C>T	XP_024303484.1:n.1219-722C>T
XM_024447717.1:c.1139-722C>T	XP_024303485.1:n.1139-722C>T
XR_002956828.1:n.1234-722C>T
XR_002956829.1:n.1154-722C>T
XR_002956830.1:n.2314C>T
XR_002956831.1:n.1989C>T
XR_002956832.1:n.1313C>T
NM_012203.2:c.894C>T MANE Select	NP_036335.1:p.Thr298=