Canonical Allele Identifier: CA341392169
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539602-C-A
MyVariant Identifiers: chr1:g.101005158C>A (hg19) chr1:g.100539602C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539602C>A , CM000663.2:g.100539602C>A GRCh38
NC_000001.10:g.101005158C>A , CM000663.1:g.101005158C>A GRCh37
NC_000001.9:g.100777746C>A NCBI36
NG_053134.1:g.6431C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.636C>A MANE Select ENSP00000314223.4:p.Tyr212Ter
ENST00000315033.4:c.636C>A ENSP00000314223.4:p.Tyr212Ter
NM_022049.2:c.636C>A NP_071332.2:p.Tyr212Ter
NM_022049.3:c.636C>A MANE Select NP_071332.2:p.Tyr212Ter
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