Canonical Allele Identifier: CA465004088

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429766C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429769C>T , CM000671.2:g.37429769C>T	GRCh38
NC_000009.11:g.37429766C>T , CM000671.1:g.37429766C>T	GRCh37
NC_000009.10:g.37419766C>T	NCBI36
NG_008135.1:g.12060C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.531C>T MANE Select	ENSP00000313432.6:p.Val177=
ENST00000318158.10:c.531C>T	ENSP00000313432.6:p.Val177=
ENST00000377824.8:n.568C>T
ENST00000460882.5:n.558C>T
ENST00000480596.5:n.1232C>T
ENST00000491488.5:n.236C>T
ENST00000494290.1:c.102C>T	ENSP00000432021.1:p.Val34=
ENST00000497693.1:n.2064C>T
ENST00000607784.1:c.531C>T	ENSP00000475569.1:p.Val177=
NM_012203.1:c.531C>T	NP_036335.1:p.Val177=
XM_005251631.1:c.210C>T	XP_005251688.1:p.Val70=
XM_011518073.1:c.129C>T	XP_011516375.1:p.Val43=
XR_929374.1:n.976C>T
XM_017015320.2:c.531C>T	XP_016870809.1:p.Val177=
XM_017015321.2:c.531C>T	XP_016870810.1:p.Val177=
XM_017015323.2:c.129C>T	XP_016870812.1:p.Val43=
XM_024447716.1:c.804C>T	XP_024303484.1:p.Val268=
XM_024447717.1:c.804C>T	XP_024303485.1:p.Val268=
XR_002956828.1:n.819C>T
XR_002956829.1:n.819C>T
XR_002956830.1:n.590C>T
XR_002956831.1:n.265C>T
XR_002956832.1:n.950C>T
NM_012203.2:c.531C>T MANE Select	NP_036335.1:p.Val177=