Canonical Allele Identifier: CA663230661
Gene: GPR158 HGNC NCBI

Linked Data

dbSNP Id: rs996441521

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.25591545G>C , CM000672.2:g.25591545G>C GRCh38
NC_000010.10:g.25880474G>C , CM000672.1:g.25880474G>C GRCh37
NC_000010.9:g.25920480G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376351.4:c.1892+2400G>C MANE Select ENSP00000365529.3:n.1892+2400G>C
ENST00000650135.1:c.1655+2400G>C ENSP00000498176.1:n.1655+2400G>C
ENST00000376351.3:c.1892+2400G>C ENSP00000365529.3:n.1892+2400G>C
NM_020752.2:c.1892+2400G>C NP_065803.2:n.1892+2400G>C
XR_930511.1:n.2576+2400G>C
XR_930512.1:n.2576+2400G>C
XM_017016452.2:c.332+2400G>C XP_016871941.1:n.332+2400G>C
XR_930512.3:n.2576+2400G>C
NM_020752.3:c.1892+2400G>C MANE Select NP_065803.2:n.1892+2400G>C