Canonical Allele Identifier: CA449629345
Gene: USP8P1 HGNC NCBI

Linked Data

gnomAD v4: 6-31277568-A-C
MyVariant Identifiers: chr6:g.31245345A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277568A>C , CM000668.2:g.31277568A>C GRCh38
NC_000006.11:g.31245345A>C , CM000668.1:g.31245345A>C GRCh37
NC_000006.10:g.31353324A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000494673.1:n.1997A>C