Canonical Allele Identifier: CA341392985
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539995-C-A
MyVariant Identifiers: chr1:g.101005551C>A (hg19) chr1:g.100539995C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539995C>A , CM000663.2:g.100539995C>A GRCh38
NC_000001.10:g.101005551C>A , CM000663.1:g.101005551C>A GRCh37
NC_000001.9:g.100778139C>A NCBI36
NG_053134.1:g.6824C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1029C>A MANE Select ENSP00000314223.4:p.Phe343Leu
ENST00000315033.4:c.1029C>A ENSP00000314223.4:p.Phe343Leu
NM_022049.2:c.1029C>A NP_071332.2:p.Phe343Leu
NM_022049.3:c.1029C>A MANE Select NP_071332.2:p.Phe343Leu
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