Canonical Allele Identifier: CA254038906
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs9546697

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458230G>A , CM000675.2:g.84458230G>A GRCh38
NC_000013.10:g.85032365G>A , CM000675.1:g.85032365G>A GRCh37
NC_000013.9:g.83930366G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104134G>A
XR_942133.1:n.369-46311C>T
XR_942134.1:n.366-46311C>T