Canonical Allele Identifier: CA373443327

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429761G>C (hg19) ; chr9:g.37429764G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429764G>C , CM000671.2:g.37429764G>C	GRCh38
NC_000009.11:g.37429761G>C , CM000671.1:g.37429761G>C	GRCh37
NC_000009.10:g.37419761G>C	NCBI36
NG_008135.1:g.12055G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.526G>C MANE Select	ENSP00000313432.6:p.Gly176Arg
ENST00000318158.10:c.526G>C	ENSP00000313432.6:p.Gly176Arg
ENST00000377824.8:n.563G>C
ENST00000460882.5:n.553G>C
ENST00000480596.5:n.1227G>C
ENST00000491488.5:n.231G>C
ENST00000494290.1:c.97G>C	ENSP00000432021.1:p.Gly33Arg
ENST00000497693.1:n.2059G>C
ENST00000607784.1:c.526G>C	ENSP00000475569.1:p.Gly176Arg
NM_012203.1:c.526G>C	NP_036335.1:p.Gly176Arg
XM_005251631.1:c.205G>C	XP_005251688.1:p.Gly69Arg
XM_011518073.1:c.124G>C	XP_011516375.1:p.Gly42Arg
XR_929374.1:n.971G>C
XM_017015320.2:c.526G>C	XP_016870809.1:p.Gly176Arg
XM_017015321.2:c.526G>C	XP_016870810.1:p.Gly176Arg
XM_017015323.2:c.124G>C	XP_016870812.1:p.Gly42Arg
XM_024447716.1:c.799G>C	XP_024303484.1:p.Gly267Arg
XM_024447717.1:c.799G>C	XP_024303485.1:p.Gly267Arg
XR_002956828.1:n.814G>C
XR_002956829.1:n.814G>C
XR_002956830.1:n.585G>C
XR_002956831.1:n.260G>C
XR_002956832.1:n.945G>C
NM_012203.2:c.526G>C MANE Select	NP_036335.1:p.Gly176Arg