Canonical Allele Identifier: CA1184190864
Gene: GPR88 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539593G= , CM000663.2:g.100539593G= GRCh38
NC_000001.10:g.101005149G= , CM000663.1:g.101005149G= GRCh37
NC_000001.9:g.100777737G= NCBI36
NG_053134.1:g.6422G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.627G= MANE Select ENSP00000314223.4:p.Leu209=
ENST00000315033.4:c.627G= ENSP00000314223.4:p.Leu209=
NM_022049.2:c.627G= NP_071332.2:p.Leu209=
NM_022049.3:c.627G= MANE Select NP_071332.2:p.Leu209=
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