Canonical Allele Identifier: CA449629383
Gene: USP8P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31245349C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277572C>T , CM000668.2:g.31277572C>T GRCh38
NC_000006.11:g.31245349C>T , CM000668.1:g.31245349C>T GRCh37
NC_000006.10:g.31353328C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000494673.1:n.2001C>T