Canonical Allele Identifier: CA587803183

Gene: GRHPR

Linked Data

• dbSNP Id: rs1479943959
• gnomAD v2: 9-37422699-C-T
• gnomAD v4: 9-37422702-C-T
• MyVariant Identifiers: chr9:g.37422699C>T (hg19) ; chr9:g.37422702C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37422702C>T , CM000671.2:g.37422702C>T	GRCh38
NC_000009.11:g.37422699C>T , CM000671.1:g.37422699C>T	GRCh37
NC_000009.10:g.37412699C>T	NCBI36
NG_008135.1:g.4993C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.-49C>T MANE Select	ENSP00000313432.6:n.-49C>T
ENST00000318158.10:c.-49C>T	ENSP00000313432.6:n.-49C>T
ENST00000460882.5:n.7C>T
ENST00000493368.5:n.37C>T
XM_005251631.1:c.-49C>T	XP_005251688.1:n.-49C>T
XR_929374.1:n.37C>T
XM_017015320.2:c.-49C>T	XP_016870809.1:n.-49C>T
XM_017015321.2:c.-49C>T	XP_016870810.1:n.-49C>T
XM_017015323.2:c.-811C>T	XP_016870812.1:n.-811C>T
XM_024447716.1:c.253C>T	XP_024303484.1:p.Pro85Ser
XM_024447717.1:c.253C>T	XP_024303485.1:p.Pro85Ser
XR_002956828.1:n.268C>T
XR_002956829.1:n.268C>T
XR_002956830.1:n.11C>T
XR_002956831.1:n.7C>T
XR_002956832.1:n.11C>T
NM_012203.2:c.-49C>T MANE Select	NP_036335.1:n.-49C>T