Canonical Allele Identifier: CA192896399

Gene: GRHPR

Linked Data

• dbSNP Id: rs929154649
• MyVariant Identifiers: chr9:g.37437037C>G (hg19) ; chr9:g.37437040C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37437040C>G , CM000671.2:g.37437040C>G	GRCh38
NC_000009.11:g.37437037C>G , CM000671.1:g.37437037C>G	GRCh37
NC_000009.10:g.37427037C>G	NCBI36
NG_008135.1:g.19331C>G

Transcript Alleles

HGVS	Amino-acid Change
XM_017015320.2:c.946-371C>G	XP_016870809.1:n.946-371C>G
XM_017015321.2:c.866-371C>G	XP_016870810.1:n.866-371C>G
XM_017015323.2:c.544-371C>G	XP_016870812.1:n.544-371C>G
XM_024447716.1:c.1219-371C>G	XP_024303484.1:n.1219-371C>G
XM_024447717.1:c.1139-371C>G	XP_024303485.1:n.1139-371C>G
XR_002956828.1:n.1234-371C>G
XR_002956829.1:n.1154-371C>G