Canonical Allele Identifier: CA341392216
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539627-G-T
MyVariant Identifiers: chr1:g.101005183G>T (hg19) chr1:g.100539627G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539627G>T , CM000663.2:g.100539627G>T GRCh38
NC_000001.10:g.101005183G>T , CM000663.1:g.101005183G>T GRCh37
NC_000001.9:g.100777771G>T NCBI36
NG_053134.1:g.6456G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.661G>T MANE Select ENSP00000314223.4:p.Val221Phe
ENST00000315033.4:c.661G>T ENSP00000314223.4:p.Val221Phe
NM_022049.2:c.661G>T NP_071332.2:p.Val221Phe
NM_022049.3:c.661G>T MANE Select NP_071332.2:p.Val221Phe
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