Canonical Allele Identifier: CA1619083360
Gene: USP8P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277575A= , CM000668.2:g.31277575A= GRCh38
NC_000006.11:g.31245352A= , CM000668.1:g.31245352A= GRCh37
NC_000006.10:g.31353331A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000494673.1:n.2004A=