Canonical Allele Identifier: CA449629354
Gene: USP8P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31245346T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277569T>A , CM000668.2:g.31277569T>A GRCh38
NC_000006.11:g.31245346T>A , CM000668.1:g.31245346T>A GRCh37
NC_000006.10:g.31353325T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000494673.1:n.1998T>A