Canonical Allele Identifier: CA2689984738

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436993-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436993C>T , CM000671.2:g.37436993C>T	GRCh38
NC_000009.11:g.37436990C>T , CM000671.1:g.37436990C>T	GRCh37
NC_000009.10:g.37426990C>T	NCBI36
NG_008135.1:g.19284C>T

Transcript Alleles

HGVS	Amino-acid Change
XM_005251631.1:c.*211C>T	XP_005251688.1:n.*211C>T
XM_011518073.1:c.*211C>T	XP_011516375.1:n.*211C>T
XM_017015320.2:c.946-418C>T	XP_016870809.1:n.946-418C>T
XM_017015321.2:c.866-418C>T	XP_016870810.1:n.866-418C>T
XM_017015323.2:c.544-418C>T	XP_016870812.1:n.544-418C>T
XM_024447716.1:c.1219-418C>T	XP_024303484.1:n.1219-418C>T
XM_024447717.1:c.1139-418C>T	XP_024303485.1:n.1139-418C>T
XR_002956828.1:n.1234-418C>T
XR_002956829.1:n.1154-418C>T
XR_002956830.1:n.2618C>T
XR_002956831.1:n.2293C>T
XR_002956832.1:n.1617C>T