Canonical Allele Identifier: CA863723594

Gene: GRHPR

Linked Data

• dbSNP Id: rs1381253727
• gnomAD v4: 9-37436998-T-C
• MyVariant Identifiers: chr9:g.37436995T>C (hg19) ; chr9:g.37436998T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436998T>C , CM000671.2:g.37436998T>C	GRCh38
NC_000009.11:g.37436995T>C , CM000671.1:g.37436995T>C	GRCh37
NC_000009.10:g.37426995T>C	NCBI36
NG_008135.1:g.19289T>C

Transcript Alleles

HGVS	Amino-acid Change
XM_017015320.2:c.946-413T>C	XP_016870809.1:n.946-413T>C
XM_017015321.2:c.866-413T>C	XP_016870810.1:n.866-413T>C
XM_017015323.2:c.544-413T>C	XP_016870812.1:n.544-413T>C
XM_024447716.1:c.1219-413T>C	XP_024303484.1:n.1219-413T>C
XM_024447717.1:c.1139-413T>C	XP_024303485.1:n.1139-413T>C
XR_002956828.1:n.1234-413T>C
XR_002956829.1:n.1154-413T>C