Canonical Allele Identifier: CA863723567

Gene: GRHPR

Linked Data

• dbSNP Id: rs1301675101
• MyVariant Identifiers: chr9:g.37436984G>A (hg19) ; chr9:g.37436987G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436987G>A , CM000671.2:g.37436987G>A	GRCh38
NC_000009.11:g.37436984G>A , CM000671.1:g.37436984G>A	GRCh37
NC_000009.10:g.37426984G>A	NCBI36
NG_008135.1:g.19278G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*205G>A MANE Select	ENSP00000313432.6:n.*205G>A
ENST00000318158.10:c.*205G>A	ENSP00000313432.6:n.*205G>A
ENST00000480596.5:n.1893G>A
ENST00000494290.1:c.*158G>A	ENSP00000432021.1:n.*158G>A
ENST00000497693.1:n.4760G>A
NM_012203.1:c.*205G>A	NP_036335.1:n.*205G>A
XM_005251631.1:c.*205G>A	XP_005251688.1:n.*205G>A
XM_011518073.1:c.*205G>A	XP_011516375.1:n.*205G>A
XM_017015320.2:c.946-424G>A	XP_016870809.1:n.946-424G>A
XM_017015321.2:c.866-424G>A	XP_016870810.1:n.866-424G>A
XM_017015323.2:c.544-424G>A	XP_016870812.1:n.544-424G>A
XM_024447716.1:c.1219-424G>A	XP_024303484.1:n.1219-424G>A
XM_024447717.1:c.1139-424G>A	XP_024303485.1:n.1139-424G>A
XR_002956828.1:n.1234-424G>A
XR_002956829.1:n.1154-424G>A
XR_002956830.1:n.2612G>A
XR_002956831.1:n.2287G>A
XR_002956832.1:n.1611G>A
NM_012203.2:c.*205G>A MANE Select	NP_036335.1:n.*205G>A