Canonical Allele Identifier: CA2721314196

Gene: GPR158

Linked Data

• dbSNP Id: rs2130658762

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.25501885G>C , CM000672.2:g.25501885G>C	GRCh38
NC_000010.10:g.25790814G>C , CM000672.1:g.25790814G>C	GRCh37
NC_000010.9:g.25830820G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376351.4:c.1404+35166G>C MANE Select	ENSP00000365529.3:n.1404+35166G>C
ENST00000650135.1:c.1167+35166G>C	ENSP00000498176.1:n.1167+35166G>C
ENST00000376351.3:c.1404+35166G>C	ENSP00000365529.3:n.1404+35166G>C
NM_020752.2:c.1404+35166G>C	NP_065803.2:n.1404+35166G>C
XR_930511.1:n.2088+35166G>C
XR_930512.1:n.2088+35166G>C
XM_017016452.2:c.-157+35166G>C	XP_016871941.1:n.-157+35166G>C
XR_930512.3:n.2088+35166G>C
NM_020752.3:c.1404+35166G>C MANE Select	NP_065803.2:n.1404+35166G>C