Canonical Allele Identifier: CA373443362

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429771G>C (hg19) ; chr9:g.37429774G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429774G>C , CM000671.2:g.37429774G>C	GRCh38
NC_000009.11:g.37429771G>C , CM000671.1:g.37429771G>C	GRCh37
NC_000009.10:g.37419771G>C	NCBI36
NG_008135.1:g.12065G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.536G>C MANE Select	ENSP00000313432.6:p.Arg179Thr
ENST00000318158.10:c.536G>C	ENSP00000313432.6:p.Arg179Thr
ENST00000377824.8:n.573G>C
ENST00000460882.5:n.563G>C
ENST00000480596.5:n.1237G>C
ENST00000491488.5:n.241G>C
ENST00000494290.1:c.107G>C	ENSP00000432021.1:p.Arg36Thr
ENST00000497693.1:n.2069G>C
ENST00000607784.1:c.536G>C	ENSP00000475569.1:p.Arg179Thr
NM_012203.1:c.536G>C	NP_036335.1:p.Arg179Thr
XM_005251631.1:c.215G>C	XP_005251688.1:p.Arg72Thr
XM_011518073.1:c.134G>C	XP_011516375.1:p.Arg45Thr
XR_929374.1:n.981G>C
XM_017015320.2:c.536G>C	XP_016870809.1:p.Arg179Thr
XM_017015321.2:c.536G>C	XP_016870810.1:p.Arg179Thr
XM_017015323.2:c.134G>C	XP_016870812.1:p.Arg45Thr
XM_024447716.1:c.809G>C	XP_024303484.1:p.Arg270Thr
XM_024447717.1:c.809G>C	XP_024303485.1:p.Arg270Thr
XR_002956828.1:n.824G>C
XR_002956829.1:n.824G>C
XR_002956830.1:n.595G>C
XR_002956831.1:n.270G>C
XR_002956832.1:n.955G>C
NM_012203.2:c.536G>C MANE Select	NP_036335.1:p.Arg179Thr