Canonical Allele Identifier: CA801200926
Gene: LINC02213 HGNC NCBI

Linked Data

dbSNP Id: rs1354867210
MyVariant Identifiers: chr5:g.10512607C>T (hg19) chr5:g.10512495C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10512495C>T , CM000667.2:g.10512495C>T GRCh38
NC_000005.9:g.10512607C>T , CM000667.1:g.10512607C>T GRCh37
NC_000005.8:g.10565607C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_134289.1:n.330-5920G>A
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