Canonical Allele Identifier: CA2689984748

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37437002-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37437002C>T , CM000671.2:g.37437002C>T	GRCh38
NC_000009.11:g.37436999C>T , CM000671.1:g.37436999C>T	GRCh37
NC_000009.10:g.37426999C>T	NCBI36
NG_008135.1:g.19293C>T

Transcript Alleles

HGVS	Amino-acid Change
XM_017015320.2:c.946-409C>T	XP_016870809.1:n.946-409C>T
XM_017015321.2:c.866-409C>T	XP_016870810.1:n.866-409C>T
XM_017015323.2:c.544-409C>T	XP_016870812.1:n.544-409C>T
XM_024447716.1:c.1219-409C>T	XP_024303484.1:n.1219-409C>T
XM_024447717.1:c.1139-409C>T	XP_024303485.1:n.1139-409C>T
XR_002956828.1:n.1234-409C>T
XR_002956829.1:n.1154-409C>T