Canonical Allele Identifier: CA449629439
Gene: USP8P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31245354G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277577G>C , CM000668.2:g.31277577G>C GRCh38
NC_000006.11:g.31245354G>C , CM000668.1:g.31245354G>C GRCh37
NC_000006.10:g.31353333G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000494673.1:n.2006G>C