Canonical Allele Identifier: CA449629339
Gene: USP8P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31245344T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277567T>C , CM000668.2:g.31277567T>C GRCh38
NC_000006.11:g.31245344T>C , CM000668.1:g.31245344T>C GRCh37
NC_000006.10:g.31353323T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000494673.1:n.1996T>C