Canonical Allele Identifier: CA5058917
Gene: GRHPR HGNC NCBI

Linked Data

dbSNP Id: rs200089195
gnomAD v2: 9-37424819-T-C
gnomAD v3: 9-37424822-T-C
gnomAD v4: 9-37424822-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37424822T>C , CM000671.2:g.37424822T>C GRCh38
NC_000009.11:g.37424819T>C , CM000671.1:g.37424819T>C GRCh37
NC_000009.10:g.37414819T>C NCBI36
NG_008135.1:g.7113T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.84-23T>C MANE Select ENSP00000313432.6:n.84-23T>C
ENST00000318158.10:c.84-23T>C ENSP00000313432.6:n.84-23T>C
ENST00000377824.8:n.121-23T>C
ENST00000460882.5:n.111-23T>C
ENST00000487399.5:n.93-23T>C
ENST00000491488.5:n.109+1989T>C
ENST00000493368.5:n.141-23T>C
ENST00000607784.1:c.84-23T>C ENSP00000475569.1:n.84-23T>C
NM_012203.1:c.84-23T>C NP_036335.1:n.84-23T>C
XM_005251631.1:c.83+1989T>C XP_005251688.1:n.83+1989T>C
XM_011518073.1:c.-679-23T>C XP_011516375.1:n.-679-23T>C
XR_929374.1:n.169-23T>C
XM_017015320.2:c.84-23T>C XP_016870809.1:n.84-23T>C
XM_017015321.2:c.84-23T>C XP_016870810.1:n.84-23T>C
XM_017015323.2:c.-679-23T>C XP_016870812.1:n.-679-23T>C
XM_024447716.1:c.357-23T>C XP_024303484.1:n.357-23T>C
XM_024447717.1:c.357-23T>C XP_024303485.1:n.357-23T>C
XR_002956828.1:n.372-23T>C
XR_002956829.1:n.372-23T>C
XR_002956830.1:n.143-23T>C
XR_002956831.1:n.138+1989T>C
XR_002956832.1:n.143-23T>C
NM_012203.2:c.84-23T>C MANE Select NP_036335.1:n.84-23T>C