ClinGen Allele Registry
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Canonical Allele Identifier:
CA449630316
Gene: USP8P1
HGNC
NCBI
Linked Data
gnomAD v4:
6-31277671-G-A
MyVariant Identifiers:
chr6:g.31245448G>A (hg19)
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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
Search 100 bp 5'
Search 100 bp 3'