Canonical Allele Identifier: CA204369517
Gene: GPR158 HGNC NCBI

Linked Data

dbSNP Id: rs996441521
gnomAD v2: 10-25880474-G-A
gnomAD v3: 10-25591545-G-A
gnomAD v4: 10-25591545-G-A
MyVariant Identifiers: chr10:g.25880474G>A (hg19) chr10:g.25591545G>A (hg38)
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Genomic Alleles

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

Transcript Alleles

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