Canonical Allele Identifier: CA587805603

Gene: GRHPR

Linked Data

• dbSNP Id: rs1281679152
• gnomAD v2: 9-37437025-G-C
• gnomAD v3: 9-37437028-G-C
• gnomAD v4: 9-37437028-G-C
• MyVariant Identifiers: chr9:g.37437025G>C (hg19) ; chr9:g.37437028G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37437028G>C , CM000671.2:g.37437028G>C	GRCh38
NC_000009.11:g.37437025G>C , CM000671.1:g.37437025G>C	GRCh37
NC_000009.10:g.37427025G>C	NCBI36
NG_008135.1:g.19319G>C

Transcript Alleles

HGVS	Amino-acid Change
XM_017015320.2:c.946-383G>C	XP_016870809.1:n.946-383G>C
XM_017015321.2:c.866-383G>C	XP_016870810.1:n.866-383G>C
XM_017015323.2:c.544-383G>C	XP_016870812.1:n.544-383G>C
XM_024447716.1:c.1219-383G>C	XP_024303484.1:n.1219-383G>C
XM_024447717.1:c.1139-383G>C	XP_024303485.1:n.1139-383G>C
XR_002956828.1:n.1234-383G>C
XR_002956829.1:n.1154-383G>C