Canonical Allele Identifier: CA373442609
Gene: GRHPR HGNC NCBI

Linked Data

dbSNP Id: rs1588752847
gnomAD v4: 9-37426633-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37426633A>G , CM000671.2:g.37426633A>G GRCh38
NC_000009.11:g.37426630A>G , CM000671.1:g.37426630A>G GRCh37
NC_000009.10:g.37416630A>G NCBI36
NG_008135.1:g.8924A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.383A>G MANE Select ENSP00000313432.6:p.Glu128Gly
ENST00000318158.10:c.383A>G ENSP00000313432.6:p.Glu128Gly
ENST00000377824.8:n.420A>G
ENST00000460882.5:n.410A>G
ENST00000487399.5:n.935A>G
ENST00000491488.5:n.110-1851A>G
ENST00000493368.5:n.440A>G
ENST00000607784.1:c.383A>G ENSP00000475569.1:p.Glu128Gly
NM_012203.1:c.383A>G NP_036335.1:p.Glu128Gly
XM_005251631.1:c.84-1851A>G XP_005251688.1:n.84-1851A>G
XM_011518073.1:c.-380A>G XP_011516375.1:n.-380A>G
XR_929374.1:n.468A>G
XM_017015320.2:c.383A>G XP_016870809.1:p.Glu128Gly
XM_017015321.2:c.383A>G XP_016870810.1:p.Glu128Gly
XM_017015323.2:c.-380A>G XP_016870812.1:n.-380A>G
XM_024447716.1:c.656A>G XP_024303484.1:p.Glu219Gly
XM_024447717.1:c.656A>G XP_024303485.1:p.Glu219Gly
XR_002956828.1:n.671A>G
XR_002956829.1:n.671A>G
XR_002956830.1:n.442A>G
XR_002956831.1:n.139-1851A>G
XR_002956832.1:n.442A>G
NM_012203.2:c.383A>G MANE Select NP_036335.1:p.Glu128Gly