Canonical Allele Identifier: CA900877372
Gene: LINC02006 HGNC NCBI

Linked Data

dbSNP Id: rs1228757446
MyVariant Identifiers: chr3:g.153350087C>T (hg19) chr3:g.153632298C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153632298C>T , CM000665.2:g.153632298C>T GRCh38
NC_000003.11:g.153350087C>T , CM000665.1:g.153350087C>T GRCh37
NC_000003.10:g.154832777C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924593.1:n.363-27553G>A
XR_924594.1:n.60+25772G>A
NR_146713.1:n.161-27553G>A
Search 100 bp 5'
Search 100 bp 3'