Canonical Allele Identifier: CA652908550
Gene: GRHPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37429676T>G , CM000671.2:g.37429676T>G GRCh38
NC_000009.11:g.37429673T>G , CM000671.1:g.37429673T>G GRCh37
NC_000009.10:g.37419673T>G NCBI36
NG_008135.1:g.11967T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.494-56T>G MANE Select ENSP00000313432.6:n.494-56T>G
ENST00000318158.10:c.494-56T>G ENSP00000313432.6:n.494-56T>G
ENST00000377824.8:n.531-56T>G
ENST00000460882.5:n.521-56T>G
ENST00000480596.5:n.1139T>G
ENST00000491488.5:n.199-56T>G
ENST00000494290.1:c.9T>G ENSP00000432021.1:p.Gly3=
ENST00000497693.1:n.1971T>G
ENST00000607784.1:c.494-56T>G ENSP00000475569.1:n.494-56T>G
NM_012203.1:c.494-56T>G NP_036335.1:n.494-56T>G
XM_005251631.1:c.173-56T>G XP_005251688.1:n.173-56T>G
XM_011518073.1:c.92-56T>G XP_011516375.1:n.92-56T>G
XR_929374.1:n.939-56T>G
XM_017015320.2:c.494-56T>G XP_016870809.1:n.494-56T>G
XM_017015321.2:c.494-56T>G XP_016870810.1:n.494-56T>G
XM_017015323.2:c.92-56T>G XP_016870812.1:n.92-56T>G
XM_024447716.1:c.767-56T>G XP_024303484.1:n.767-56T>G
XM_024447717.1:c.767-56T>G XP_024303485.1:n.767-56T>G
XR_002956828.1:n.782-56T>G
XR_002956829.1:n.782-56T>G
XR_002956830.1:n.553-56T>G
XR_002956831.1:n.228-56T>G
XR_002956832.1:n.913-56T>G
NM_012203.2:c.494-56T>G MANE Select NP_036335.1:n.494-56T>G