Canonical Allele Identifier: CA2107004921
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1879680443
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458009G>A , CM000675.2:g.84458009G>A GRCh38
NC_000013.10:g.85032144G>A , CM000675.1:g.85032144G>A GRCh37
NC_000013.9:g.83930145G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104355G>A
XR_942133.1:n.369-46090C>T
XR_942134.1:n.366-46090C>T
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