Canonical Allele Identifier: CA449629305
Gene: USP8P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31245341A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277564A>C , CM000668.2:g.31277564A>C GRCh38
NC_000006.11:g.31245341A>C , CM000668.1:g.31245341A>C GRCh37
NC_000006.10:g.31353320A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000494673.1:n.1993A>C