Canonical Allele Identifier: CA1619083420
Gene: USP8P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277658G= , CM000668.2:g.31277658G= GRCh38
NC_000006.11:g.31245435G= , CM000668.1:g.31245435G= GRCh37
NC_000006.10:g.31353414G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000494673.1:n.2087G=