Canonical Allele Identifier: CA449629300
Gene: USP8P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31245340C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277563C>T , CM000668.2:g.31277563C>T GRCh38
NC_000006.11:g.31245340C>T , CM000668.1:g.31245340C>T GRCh37
NC_000006.10:g.31353319C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000494673.1:n.1992C>T
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