Canonical Allele Identifier: CA373443278

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429746C>G (hg19) ; chr9:g.37429749C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429749C>G , CM000671.2:g.37429749C>G	GRCh38
NC_000009.11:g.37429746C>G , CM000671.1:g.37429746C>G	GRCh37
NC_000009.10:g.37419746C>G	NCBI36
NG_008135.1:g.12040C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.511C>G MANE Select	ENSP00000313432.6:p.Arg171Gly
ENST00000318158.10:c.511C>G	ENSP00000313432.6:p.Arg171Gly
ENST00000377824.8:n.548C>G
ENST00000460882.5:n.538C>G
ENST00000480596.5:n.1212C>G
ENST00000491488.5:n.216C>G
ENST00000494290.1:c.82C>G	ENSP00000432021.1:p.Arg28Gly
ENST00000497693.1:n.2044C>G
ENST00000607784.1:c.511C>G	ENSP00000475569.1:p.Arg171Gly
NM_012203.1:c.511C>G	NP_036335.1:p.Arg171Gly
XM_005251631.1:c.190C>G	XP_005251688.1:p.Arg64Gly
XM_011518073.1:c.109C>G	XP_011516375.1:p.Arg37Gly
XR_929374.1:n.956C>G
XM_017015320.2:c.511C>G	XP_016870809.1:p.Arg171Gly
XM_017015321.2:c.511C>G	XP_016870810.1:p.Arg171Gly
XM_017015323.2:c.109C>G	XP_016870812.1:p.Arg37Gly
XM_024447716.1:c.784C>G	XP_024303484.1:p.Arg262Gly
XM_024447717.1:c.784C>G	XP_024303485.1:p.Arg262Gly
XR_002956828.1:n.799C>G
XR_002956829.1:n.799C>G
XR_002956830.1:n.570C>G
XR_002956831.1:n.245C>G
XR_002956832.1:n.930C>G
NM_012203.2:c.511C>G MANE Select	NP_036335.1:p.Arg171Gly