Canonical Allele Identifier: CA2689981175
Gene: GRHPR HGNC NCBI

Linked Data

gnomAD v4: 9-37429557-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37429557G>T , CM000671.2:g.37429557G>T GRCh38
NC_000009.11:g.37429554G>T , CM000671.1:g.37429554G>T GRCh37
NC_000009.10:g.37419554G>T NCBI36
NG_008135.1:g.11848G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.494-175G>T MANE Select ENSP00000313432.6:n.494-175G>T
ENST00000318158.10:c.494-175G>T ENSP00000313432.6:n.494-175G>T
ENST00000377824.8:n.531-175G>T
ENST00000460882.5:n.521-175G>T
ENST00000480596.5:n.1020G>T
ENST00000491488.5:n.199-175G>T
ENST00000494290.1:c.-111G>T ENSP00000432021.1:n.-111G>T
ENST00000497693.1:n.1852G>T
ENST00000607784.1:c.494-175G>T ENSP00000475569.1:n.494-175G>T
NM_012203.1:c.494-175G>T NP_036335.1:n.494-175G>T
XM_005251631.1:c.173-175G>T XP_005251688.1:n.173-175G>T
XM_011518073.1:c.92-175G>T XP_011516375.1:n.92-175G>T
XR_929374.1:n.939-175G>T
XM_017015320.2:c.494-175G>T XP_016870809.1:n.494-175G>T
XM_017015321.2:c.494-175G>T XP_016870810.1:n.494-175G>T
XM_017015323.2:c.92-175G>T XP_016870812.1:n.92-175G>T
XM_024447716.1:c.767-175G>T XP_024303484.1:n.767-175G>T
XM_024447717.1:c.767-175G>T XP_024303485.1:n.767-175G>T
XR_002956828.1:n.782-175G>T
XR_002956829.1:n.782-175G>T
XR_002956830.1:n.553-175G>T
XR_002956831.1:n.228-175G>T
XR_002956832.1:n.913-175G>T
NM_012203.2:c.494-175G>T MANE Select NP_036335.1:n.494-175G>T