Canonical Allele Identifier: CA863718744

Gene: GRHPR

Linked Data

• dbSNP Id: rs1187984689
• gnomAD v3: 9-37429705-A-G
• gnomAD v4: 9-37429705-A-G
• MyVariant Identifiers: chr9:g.37429702A>G (hg19) ; chr9:g.37429705A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429705A>G , CM000671.2:g.37429705A>G	GRCh38
NC_000009.11:g.37429702A>G , CM000671.1:g.37429702A>G	GRCh37
NC_000009.10:g.37419702A>G	NCBI36
NG_008135.1:g.11996A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.494-27A>G MANE Select	ENSP00000313432.6:n.494-27A>G
ENST00000318158.10:c.494-27A>G	ENSP00000313432.6:n.494-27A>G
ENST00000377824.8:n.531-27A>G
ENST00000460882.5:n.521-27A>G
ENST00000480596.5:n.1168A>G
ENST00000491488.5:n.199-27A>G
ENST00000494290.1:c.38A>G	ENSP00000432021.1:p.Asn13Ser
ENST00000497693.1:n.2000A>G
ENST00000607784.1:c.494-27A>G	ENSP00000475569.1:n.494-27A>G
NM_012203.1:c.494-27A>G	NP_036335.1:n.494-27A>G
XM_005251631.1:c.173-27A>G	XP_005251688.1:n.173-27A>G
XM_011518073.1:c.92-27A>G	XP_011516375.1:n.92-27A>G
XR_929374.1:n.939-27A>G
XM_017015320.2:c.494-27A>G	XP_016870809.1:n.494-27A>G
XM_017015321.2:c.494-27A>G	XP_016870810.1:n.494-27A>G
XM_017015323.2:c.92-27A>G	XP_016870812.1:n.92-27A>G
XM_024447716.1:c.767-27A>G	XP_024303484.1:n.767-27A>G
XM_024447717.1:c.767-27A>G	XP_024303485.1:n.767-27A>G
XR_002956828.1:n.782-27A>G
XR_002956829.1:n.782-27A>G
XR_002956830.1:n.553-27A>G
XR_002956831.1:n.228-27A>G
XR_002956832.1:n.913-27A>G
NM_012203.2:c.494-27A>G MANE Select	NP_036335.1:n.494-27A>G