Canonical Allele Identifier: CA1619083357
Gene: USP8P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277564A= , CM000668.2:g.31277564A= GRCh38
NC_000006.11:g.31245341A= , CM000668.1:g.31245341A= GRCh37
NC_000006.10:g.31353320A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000494673.1:n.1993A=