Canonical Allele Identifier: CA1184191362
Gene: GPR88 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1027T= MANE Select ENSP00000314223.4:p.Phe343=
ENST00000315033.4:c.1027T= ENSP00000314223.4:p.Phe343=
NM_022049.2:c.1027T= NP_071332.2:p.Phe343=
NM_022049.3:c.1027T= MANE Select NP_071332.2:p.Phe343=
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