Canonical Allele Identifier: CA2719480336
Gene: GRHPR HGNC NCBI

Linked Data

dbSNP Id: rs2118862570

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37425849C>T , CM000671.2:g.37425849C>T GRCh38
NC_000009.11:g.37425846C>T , CM000671.1:g.37425846C>T GRCh37
NC_000009.10:g.37415846C>T NCBI36
NG_008135.1:g.8140C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.215-73C>T MANE Select ENSP00000313432.6:n.215-73C>T
ENST00000318158.10:c.215-73C>T ENSP00000313432.6:n.215-73C>T
ENST00000377824.8:n.252-73C>T
ENST00000460882.5:n.242-73C>T
ENST00000487399.5:n.224-73C>T
ENST00000491488.5:n.110-2635C>T
ENST00000493368.5:n.272-73C>T
ENST00000607784.1:c.215-73C>T ENSP00000475569.1:n.215-73C>T
NM_012203.1:c.215-73C>T NP_036335.1:n.215-73C>T
XM_005251631.1:c.84-2635C>T XP_005251688.1:n.84-2635C>T
XM_011518073.1:c.-548-73C>T XP_011516375.1:n.-548-73C>T
XR_929374.1:n.300-73C>T
XM_017015320.2:c.215-73C>T XP_016870809.1:n.215-73C>T
XM_017015321.2:c.215-73C>T XP_016870810.1:n.215-73C>T
XM_017015323.2:c.-548-73C>T XP_016870812.1:n.-548-73C>T
XM_024447716.1:c.488-73C>T XP_024303484.1:n.488-73C>T
XM_024447717.1:c.488-73C>T XP_024303485.1:n.488-73C>T
XR_002956828.1:n.503-73C>T
XR_002956829.1:n.503-73C>T
XR_002956830.1:n.274-73C>T
XR_002956831.1:n.139-2635C>T
XR_002956832.1:n.274-73C>T
NM_012203.2:c.215-73C>T MANE Select NP_036335.1:n.215-73C>T