Canonical Allele Identifier: CA1184190882
Gene: GPR88 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539602C= , CM000663.2:g.100539602C= GRCh38
NC_000001.10:g.101005158C= , CM000663.1:g.101005158C= GRCh37
NC_000001.9:g.100777746C= NCBI36
NG_053134.1:g.6431C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.636C= MANE Select ENSP00000314223.4:p.Tyr212=
ENST00000315033.4:c.636C= ENSP00000314223.4:p.Tyr212=
NM_022049.2:c.636C= NP_071332.2:p.Tyr212=
NM_022049.3:c.636C= MANE Select NP_071332.2:p.Tyr212=
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