Canonical Allele Identifier: CA192896392

Gene: GRHPR

Linked Data

• dbSNP Id: rs748988688
• gnomAD v4: 9-37437026-T-C
• MyVariant Identifiers: chr9:g.37437023T>C (hg19) ; chr9:g.37437026T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37437026T>C , CM000671.2:g.37437026T>C	GRCh38
NC_000009.11:g.37437023T>C , CM000671.1:g.37437023T>C	GRCh37
NC_000009.10:g.37427023T>C	NCBI36
NG_008135.1:g.19317T>C

Transcript Alleles

HGVS	Amino-acid Change
XM_017015320.2:c.946-385T>C	XP_016870809.1:n.946-385T>C
XM_017015321.2:c.866-385T>C	XP_016870810.1:n.866-385T>C
XM_017015323.2:c.544-385T>C	XP_016870812.1:n.544-385T>C
XM_024447716.1:c.1219-385T>C	XP_024303484.1:n.1219-385T>C
XM_024447717.1:c.1139-385T>C	XP_024303485.1:n.1139-385T>C
XR_002956828.1:n.1234-385T>C
XR_002956829.1:n.1154-385T>C