Canonical Allele Identifier: CA449630325
Gene: USP8P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31245449G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277672G>A , CM000668.2:g.31277672G>A GRCh38
NC_000006.11:g.31245449G>A , CM000668.1:g.31245449G>A GRCh37
NC_000006.10:g.31353428G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000494673.1:n.2101G>A