Canonical Allele Identifier: CA1619083496
Gene: USP8P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277757A= , CM000668.2:g.31277757A= GRCh38
NC_000006.11:g.31245534A= , CM000668.1:g.31245534A= GRCh37
NC_000006.10:g.31353513A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000494673.1:n.2186A=