Canonical Allele Identifier: CA449629446
Gene: USP8P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31245355C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277578C>G , CM000668.2:g.31277578C>G GRCh38
NC_000006.11:g.31245355C>G , CM000668.1:g.31245355C>G GRCh37
NC_000006.10:g.31353334C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000494673.1:n.2007C>G