Canonical Allele Identifier: CA204369527

Gene: GPR158

Linked Data

• dbSNP Id: rs1028667945
• gnomAD v3: 10-25591569-A-G
• gnomAD v4: 10-25591569-A-G
• MyVariant Identifiers: chr10:g.25880498A>G (hg19) ; chr10:g.25591569A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.25591569A>G , CM000672.2:g.25591569A>G	GRCh38
NC_000010.10:g.25880498A>G , CM000672.1:g.25880498A>G	GRCh37
NC_000010.9:g.25920504A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376351.4:c.1892+2424A>G MANE Select	ENSP00000365529.3:n.1892+2424A>G
ENST00000650135.1:c.1655+2424A>G	ENSP00000498176.1:n.1655+2424A>G
ENST00000376351.3:c.1892+2424A>G	ENSP00000365529.3:n.1892+2424A>G
NM_020752.2:c.1892+2424A>G	NP_065803.2:n.1892+2424A>G
XR_930511.1:n.2576+2424A>G
XR_930512.1:n.2576+2424A>G
XM_017016452.2:c.332+2424A>G	XP_016871941.1:n.332+2424A>G
XR_930512.3:n.2576+2424A>G
NM_020752.3:c.1892+2424A>G MANE Select	NP_065803.2:n.1892+2424A>G