Canonical Allele Identifier: CA373443415

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429785G>C (hg19) ; chr9:g.37429788G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429788G>C , CM000671.2:g.37429788G>C	GRCh38
NC_000009.11:g.37429785G>C , CM000671.1:g.37429785G>C	GRCh37
NC_000009.10:g.37419785G>C	NCBI36
NG_008135.1:g.12079G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.550G>C MANE Select	ENSP00000313432.6:p.Gly184Arg
ENST00000318158.10:c.550G>C	ENSP00000313432.6:p.Gly184Arg
ENST00000377824.8:n.587G>C
ENST00000460882.5:n.577G>C
ENST00000480596.5:n.1251G>C
ENST00000482603.1:n.3G>C
ENST00000491488.5:n.255G>C
ENST00000494290.1:c.121G>C	ENSP00000432021.1:p.Gly41Arg
ENST00000497693.1:n.2083G>C
ENST00000607784.1:c.550G>C	ENSP00000475569.1:p.Gly184Arg
NM_012203.1:c.550G>C	NP_036335.1:p.Gly184Arg
XM_005251631.1:c.229G>C	XP_005251688.1:p.Gly77Arg
XM_011518073.1:c.148G>C	XP_011516375.1:p.Gly50Arg
XR_929374.1:n.995G>C
XM_017015320.2:c.550G>C	XP_016870809.1:p.Gly184Arg
XM_017015321.2:c.550G>C	XP_016870810.1:p.Gly184Arg
XM_017015323.2:c.148G>C	XP_016870812.1:p.Gly50Arg
XM_024447716.1:c.823G>C	XP_024303484.1:p.Gly275Arg
XM_024447717.1:c.823G>C	XP_024303485.1:p.Gly275Arg
XR_002956828.1:n.838G>C
XR_002956829.1:n.838G>C
XR_002956830.1:n.609G>C
XR_002956831.1:n.284G>C
XR_002956832.1:n.969G>C
NM_012203.2:c.550G>C MANE Select	NP_036335.1:p.Gly184Arg