Canonical Allele Identifier: CA1184191026
Gene: GPR88 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539720C= , CM000663.2:g.100539720C= GRCh38
NC_000001.10:g.101005276C= , CM000663.1:g.101005276C= GRCh37
NC_000001.9:g.100777864C= NCBI36
NG_053134.1:g.6549C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.754C= MANE Select ENSP00000314223.4:p.His252=
ENST00000315033.4:c.754C= ENSP00000314223.4:p.His252=
NM_022049.2:c.754C= NP_071332.2:p.His252=
NM_022049.3:c.754C= MANE Select NP_071332.2:p.His252=
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