Canonical Allele Identifier: CA465004072

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429745G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429748G>T , CM000671.2:g.37429748G>T	GRCh38
NC_000009.11:g.37429745G>T , CM000671.1:g.37429745G>T	GRCh37
NC_000009.10:g.37419745G>T	NCBI36
NG_008135.1:g.12039G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.510G>T MANE Select	ENSP00000313432.6:p.Arg170=
ENST00000318158.10:c.510G>T	ENSP00000313432.6:p.Arg170=
ENST00000377824.8:n.547G>T
ENST00000460882.5:n.537G>T
ENST00000480596.5:n.1211G>T
ENST00000491488.5:n.215G>T
ENST00000494290.1:c.81G>T	ENSP00000432021.1:p.Arg27=
ENST00000497693.1:n.2043G>T
ENST00000607784.1:c.510G>T	ENSP00000475569.1:p.Arg170=
NM_012203.1:c.510G>T	NP_036335.1:p.Arg170=
XM_005251631.1:c.189G>T	XP_005251688.1:p.Arg63=
XM_011518073.1:c.108G>T	XP_011516375.1:p.Arg36=
XR_929374.1:n.955G>T
XM_017015320.2:c.510G>T	XP_016870809.1:p.Arg170=
XM_017015321.2:c.510G>T	XP_016870810.1:p.Arg170=
XM_017015323.2:c.108G>T	XP_016870812.1:p.Arg36=
XM_024447716.1:c.783G>T	XP_024303484.1:p.Arg261=
XM_024447717.1:c.783G>T	XP_024303485.1:p.Arg261=
XR_002956828.1:n.798G>T
XR_002956829.1:n.798G>T
XR_002956830.1:n.569G>T
XR_002956831.1:n.244G>T
XR_002956832.1:n.929G>T
NM_012203.2:c.510G>T MANE Select	NP_036335.1:p.Arg170=