Canonical Allele Identifier: CA192896371

Gene: GRHPR

Linked Data

• dbSNP Id: rs989898980
• gnomAD v3: 9-37437002-C-G
• gnomAD v4: 9-37437002-C-G
• MyVariant Identifiers: chr9:g.37436999C>G (hg19) ; chr9:g.37437002C>G (hg38)

Genomic Alleles

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

Transcript Alleles

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