Canonical Allele Identifier: CA465004002

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37428559-G-C
• MyVariant Identifiers: chr9:g.37428556G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428559G>C , CM000671.2:g.37428559G>C	GRCh38
NC_000009.11:g.37428556G>C , CM000671.1:g.37428556G>C	GRCh37
NC_000009.10:g.37418556G>C	NCBI36
NG_008135.1:g.10850G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.480G>C MANE Select	ENSP00000313432.6:p.Gly160=
ENST00000318158.10:c.480G>C	ENSP00000313432.6:p.Gly160=
ENST00000377824.8:n.517G>C
ENST00000460882.5:n.507G>C
ENST00000480596.5:n.22G>C
ENST00000491488.5:n.185G>C
ENST00000493368.5:n.537G>C
ENST00000497693.1:n.854G>C
ENST00000607784.1:c.480G>C	ENSP00000475569.1:p.Gly160=
NM_012203.1:c.480G>C	NP_036335.1:p.Gly160=
XM_005251631.1:c.159G>C	XP_005251688.1:p.Gly53=
XM_011518073.1:c.-283G>C	XP_011516375.1:n.-283G>C
XR_929374.1:n.565G>C
XM_017015320.2:c.480G>C	XP_016870809.1:p.Gly160=
XM_017015321.2:c.480G>C	XP_016870810.1:p.Gly160=
XM_017015323.2:c.-283G>C	XP_016870812.1:n.-283G>C
XM_024447716.1:c.753G>C	XP_024303484.1:p.Gly251=
XM_024447717.1:c.753G>C	XP_024303485.1:p.Gly251=
XR_002956828.1:n.768G>C
XR_002956829.1:n.768G>C
XR_002956830.1:n.539G>C
XR_002956831.1:n.214G>C
XR_002956832.1:n.539G>C
NM_012203.2:c.480G>C MANE Select	NP_036335.1:p.Gly160=