Canonical Allele Identifier: CA214617677

Gene: GRK5

Linked Data

• dbSNP Id: rs1018535861
• gnomAD v4: 10-119326485-C-T
• MyVariant Identifiers: chr10:g.119326485C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119326485C>T , CM000672.2:g.119326485C>T	GRCh38
NC_000010.10:g.121085997C>T , CM000672.1:g.121085997C>T	GRCh37
NC_000010.9:g.121075987C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000392870.3:c.53-31C>T MANE Select	ENSP00000376609.2:n.53-31C>T
ENST00000392870.2:c.53-31C>T	ENSP00000376609.2:n.53-31C>T
NM_005308.2:c.53-31C>T	NP_005299.1:n.53-31C>T
XM_005269707.1:c.53-31C>T	XP_005269764.1:n.53-31C>T
XM_005269708.1:c.53-54330C>T	XP_005269765.1:n.53-54330C>T
XM_005269707.2:c.53-31C>T	XP_005269764.1:n.53-31C>T
NM_005308.3:c.53-31C>T MANE Select	NP_005299.1:n.53-31C>T