Canonical Allele Identifier: CA341392182
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539609-A-G
MyVariant Identifiers: chr1:g.101005165A>G (hg19) chr1:g.100539609A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539609A>G , CM000663.2:g.100539609A>G GRCh38
NC_000001.10:g.101005165A>G , CM000663.1:g.101005165A>G GRCh37
NC_000001.9:g.100777753A>G NCBI36
NG_053134.1:g.6438A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.643A>G MANE Select ENSP00000314223.4:p.Ile215Val
ENST00000315033.4:c.643A>G ENSP00000314223.4:p.Ile215Val
NM_022049.2:c.643A>G NP_071332.2:p.Ile215Val
NM_022049.3:c.643A>G MANE Select NP_071332.2:p.Ile215Val
Search 100 bp 5'
Search 100 bp 3'