Canonical Allele Identifier: CA449629380
Gene: USP8P1 HGNC NCBI

Linked Data

gnomAD v4: 6-31277572-C-A
MyVariant Identifiers: chr6:g.31245349C>A (hg19)

Genomic Alleles

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

Transcript Alleles

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