Canonical Allele Identifier: CA254038887
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1015530297
gnomAD v2: 13-85032201-G-C
gnomAD v3: 13-84458066-G-C
gnomAD v4: 13-84458066-G-C
MyVariant Identifiers: chr13:g.85032201G>C (hg19) chr13:g.84458066G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458066G>C , CM000675.2:g.84458066G>C GRCh38
NC_000013.10:g.85032201G>C , CM000675.1:g.85032201G>C GRCh37
NC_000013.9:g.83930202G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104298G>C
XR_942133.1:n.369-46147C>G
XR_942134.1:n.366-46147C>G
Search 100 bp 5'
Search 100 bp 3'