Canonical Allele Identifier: CA449630316
Gene: USP8P1 HGNC NCBI

Linked Data

gnomAD v4: 6-31277671-G-A
MyVariant Identifiers: chr6:g.31245448G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277671G>A , CM000668.2:g.31277671G>A GRCh38
NC_000006.11:g.31245448G>A , CM000668.1:g.31245448G>A GRCh37
NC_000006.10:g.31353427G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000494673.1:n.2100G>A