Canonical Allele Identifier: CA341392147
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539592-T-C
MyVariant Identifiers: chr1:g.101005148T>C (hg19) chr1:g.100539592T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539592T>C , CM000663.2:g.100539592T>C GRCh38
NC_000001.10:g.101005148T>C , CM000663.1:g.101005148T>C GRCh37
NC_000001.9:g.100777736T>C NCBI36
NG_053134.1:g.6421T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.626T>C MANE Select ENSP00000314223.4:p.Leu209Pro
ENST00000315033.4:c.626T>C ENSP00000314223.4:p.Leu209Pro
NM_022049.2:c.626T>C NP_071332.2:p.Leu209Pro
NM_022049.3:c.626T>C MANE Select NP_071332.2:p.Leu209Pro
Search 100 bp 5'
Search 100 bp 3'