Canonical Allele Identifier: CA341392129
Gene: GPR88 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.101005138G>C (hg19) chr1:g.100539582G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539582G>C , CM000663.2:g.100539582G>C GRCh38
NC_000001.10:g.101005138G>C , CM000663.1:g.101005138G>C GRCh37
NC_000001.9:g.100777726G>C NCBI36
NG_053134.1:g.6411G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.616G>C MANE Select ENSP00000314223.4:p.Ala206Pro
ENST00000315033.4:c.616G>C ENSP00000314223.4:p.Ala206Pro
NM_022049.2:c.616G>C NP_071332.2:p.Ala206Pro
NM_022049.3:c.616G>C MANE Select NP_071332.2:p.Ala206Pro
Search 100 bp 5'
Search 100 bp 3'