Canonical Allele Identifier: CA1846887176
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37436998T= , CM000671.2:g.37436998T= GRCh38
NC_000009.11:g.37436995T= , CM000671.1:g.37436995T= GRCh37
NC_000009.10:g.37426995T= NCBI36
NG_008135.1:g.19289T=

Transcript Alleles

HGVS Amino-acid Change
XM_017015320.2:c.946-413T= XP_016870809.1:n.946-413T=
XM_017015321.2:c.866-413T= XP_016870810.1:n.866-413T=
XM_017015323.2:c.544-413T= XP_016870812.1:n.544-413T=
XM_024447716.1:c.1219-413T= XP_024303484.1:n.1219-413T=
XM_024447717.1:c.1139-413T= XP_024303485.1:n.1139-413T=
XR_002956828.1:n.1234-413T=
XR_002956829.1:n.1154-413T=