Canonical Allele Identifier: CA341392978
Gene: GPR88 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.101005549T>A (hg19) chr1:g.100539993T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539993T>A , CM000663.2:g.100539993T>A GRCh38
NC_000001.10:g.101005549T>A , CM000663.1:g.101005549T>A GRCh37
NC_000001.9:g.100778137T>A NCBI36
NG_053134.1:g.6822T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1027T>A MANE Select ENSP00000314223.4:p.Phe343Ile
ENST00000315033.4:c.1027T>A ENSP00000314223.4:p.Phe343Ile
NM_022049.2:c.1027T>A NP_071332.2:p.Phe343Ile
NM_022049.3:c.1027T>A MANE Select NP_071332.2:p.Phe343Ile
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