Canonical Allele Identifier: CA341392115
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539576-C-A
MyVariant Identifiers: chr1:g.101005132C>A (hg19) chr1:g.100539576C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539576C>A , CM000663.2:g.100539576C>A GRCh38
NC_000001.10:g.101005132C>A , CM000663.1:g.101005132C>A GRCh37
NC_000001.9:g.100777720C>A NCBI36
NG_053134.1:g.6405C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.610C>A MANE Select ENSP00000314223.4:p.Gln204Lys
ENST00000315033.4:c.610C>A ENSP00000314223.4:p.Gln204Lys
NM_022049.2:c.610C>A NP_071332.2:p.Gln204Lys
NM_022049.3:c.610C>A MANE Select NP_071332.2:p.Gln204Lys
Search 100 bp 5'
Search 100 bp 3'