Canonical Allele Identifier: CA419317290
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539710-G-T
MyVariant Identifiers: chr1:g.101005266G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539710G>T , CM000663.2:g.100539710G>T GRCh38
NC_000001.10:g.101005266G>T , CM000663.1:g.101005266G>T GRCh37
NC_000001.9:g.100777854G>T NCBI36
NG_053134.1:g.6539G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.744G>T MANE Select ENSP00000314223.4:p.Pro248=
ENST00000315033.4:c.744G>T ENSP00000314223.4:p.Pro248=
NM_022049.2:c.744G>T NP_071332.2:p.Pro248=
NM_022049.3:c.744G>T MANE Select NP_071332.2:p.Pro248=
Search 100 bp 5'
Search 100 bp 3'