Canonical Allele Identifier: CA214157655

Gene: GRK5 GRK5-IT1

Linked Data

• dbSNP Id: rs891671654
• gnomAD v3: 10-119210472-T-C
• gnomAD v4: 10-119210472-T-C
• MyVariant Identifiers: chr10:g.120969984T>C (hg19) ; chr10:g.119210472T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119210472T>C , CM000672.2:g.119210472T>C	GRCh38
NC_000010.10:g.120969984T>C , CM000672.1:g.120969984T>C	GRCh37
NC_000010.9:g.120959974T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000392870.3:c.52+2503T>C (GRK5) MANE Select	ENSP00000376609.2:n.52+2503T>C
ENST00000392870.2:c.52+2503T>C (GRK5)	ENSP00000376609.2:n.52+2503T>C
NM_005308.2:c.52+2503T>C (GRK5)	NP_005299.1:n.52+2503T>C
XM_005269707.1:c.52+2503T>C (GRK5)	XP_005269764.1:n.52+2503T>C
XM_005269708.1:c.52+2503T>C (GRK5)	XP_005269765.1:n.52+2503T>C
XR_246196.2:n.583-1009T>C (GRK5-IT1)
XM_005269707.2:c.52+2503T>C (GRK5)	XP_005269764.1:n.52+2503T>C
XR_246196.4:n.669-1009T>C (GRK5-IT1)
NM_005308.3:c.52+2503T>C (GRK5) MANE Select	NP_005299.1:n.52+2503T>C