Canonical Allele Identifier: CA465003846

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37426538G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37426541G>T , CM000671.2:g.37426541G>T	GRCh38
NC_000009.11:g.37426538G>T , CM000671.1:g.37426538G>T	GRCh37
NC_000009.10:g.37416538G>T	NCBI36
NG_008135.1:g.8832G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.291G>T MANE Select	ENSP00000313432.6:p.Gly97=
ENST00000318158.10:c.291G>T	ENSP00000313432.6:p.Gly97=
ENST00000377824.8:n.328G>T
ENST00000460882.5:n.318G>T
ENST00000487399.5:n.843G>T
ENST00000491488.5:n.110-1943G>T
ENST00000493368.5:n.348G>T
ENST00000607784.1:c.291G>T	ENSP00000475569.1:p.Gly97=
NM_012203.1:c.291G>T	NP_036335.1:p.Gly97=
XM_005251631.1:c.84-1943G>T	XP_005251688.1:n.84-1943G>T
XM_011518073.1:c.-472G>T	XP_011516375.1:n.-472G>T
XR_929374.1:n.376G>T
XM_017015320.2:c.291G>T	XP_016870809.1:p.Gly97=
XM_017015321.2:c.291G>T	XP_016870810.1:p.Gly97=
XM_017015323.2:c.-472G>T	XP_016870812.1:n.-472G>T
XM_024447716.1:c.564G>T	XP_024303484.1:p.Gly188=
XM_024447717.1:c.564G>T	XP_024303485.1:p.Gly188=
XR_002956828.1:n.579G>T
XR_002956829.1:n.579G>T
XR_002956830.1:n.350G>T
XR_002956831.1:n.139-1943G>T
XR_002956832.1:n.350G>T
NM_012203.2:c.291G>T MANE Select	NP_036335.1:p.Gly97=