Canonical Allele Identifier: CA1897632600
Gene: GPR158 HGNC NCBI

Linked Data

dbSNP Id: rs1837341014

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.25591549A>G , CM000672.2:g.25591549A>G GRCh38
NC_000010.10:g.25880478A>G , CM000672.1:g.25880478A>G GRCh37
NC_000010.9:g.25920484A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376351.4:c.1892+2404A>G MANE Select ENSP00000365529.3:n.1892+2404A>G
ENST00000650135.1:c.1655+2404A>G ENSP00000498176.1:n.1655+2404A>G
ENST00000376351.3:c.1892+2404A>G ENSP00000365529.3:n.1892+2404A>G
NM_020752.2:c.1892+2404A>G NP_065803.2:n.1892+2404A>G
XR_930511.1:n.2576+2404A>G
XR_930512.1:n.2576+2404A>G
XM_017016452.2:c.332+2404A>G XP_016871941.1:n.332+2404A>G
XR_930512.3:n.2576+2404A>G
NM_020752.3:c.1892+2404A>G MANE Select NP_065803.2:n.1892+2404A>G