Canonical Allele Identifier: CA465004092

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429770A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429773A>C , CM000671.2:g.37429773A>C	GRCh38
NC_000009.11:g.37429770A>C , CM000671.1:g.37429770A>C	GRCh37
NC_000009.10:g.37419770A>C	NCBI36
NG_008135.1:g.12064A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.535A>C MANE Select	ENSP00000313432.6:p.Arg179=
ENST00000318158.10:c.535A>C	ENSP00000313432.6:p.Arg179=
ENST00000377824.8:n.572A>C
ENST00000460882.5:n.562A>C
ENST00000480596.5:n.1236A>C
ENST00000491488.5:n.240A>C
ENST00000494290.1:c.106A>C	ENSP00000432021.1:p.Arg36=
ENST00000497693.1:n.2068A>C
ENST00000607784.1:c.535A>C	ENSP00000475569.1:p.Arg179=
NM_012203.1:c.535A>C	NP_036335.1:p.Arg179=
XM_005251631.1:c.214A>C	XP_005251688.1:p.Arg72=
XM_011518073.1:c.133A>C	XP_011516375.1:p.Arg45=
XR_929374.1:n.980A>C
XM_017015320.2:c.535A>C	XP_016870809.1:p.Arg179=
XM_017015321.2:c.535A>C	XP_016870810.1:p.Arg179=
XM_017015323.2:c.133A>C	XP_016870812.1:p.Arg45=
XM_024447716.1:c.808A>C	XP_024303484.1:p.Arg270=
XM_024447717.1:c.808A>C	XP_024303485.1:p.Arg270=
XR_002956828.1:n.823A>C
XR_002956829.1:n.823A>C
XR_002956830.1:n.594A>C
XR_002956831.1:n.269A>C
XR_002956832.1:n.954A>C
NM_012203.2:c.535A>C MANE Select	NP_036335.1:p.Arg179=