Canonical Allele Identifier: CA449629310
Gene: USP8P1 HGNC NCBI

Linked Data

dbSNP Id: rs1761749411
MyVariant Identifiers: chr6:g.31245341A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31277564A>G , CM000668.2:g.31277564A>G GRCh38
NC_000006.11:g.31245341A>G , CM000668.1:g.31245341A>G GRCh37
NC_000006.10:g.31353320A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000494673.1:n.1993A>G