Canonical Allele Identifier: CA341392329
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539677-G-T
MyVariant Identifiers: chr1:g.101005233G>T (hg19) chr1:g.100539677G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539677G>T , CM000663.2:g.100539677G>T GRCh38
NC_000001.10:g.101005233G>T , CM000663.1:g.101005233G>T GRCh37
NC_000001.9:g.100777821G>T NCBI36
NG_053134.1:g.6506G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.711G>T MANE Select ENSP00000314223.4:p.Leu237Phe
ENST00000315033.4:c.711G>T ENSP00000314223.4:p.Leu237Phe
NM_022049.2:c.711G>T NP_071332.2:p.Leu237Phe
NM_022049.3:c.711G>T MANE Select NP_071332.2:p.Leu237Phe
Search 100 bp 5'
Search 100 bp 3'