Canonical Allele Identifier: CA137815813
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs996586090
MyVariant Identifiers: chr6:g.40321981C>T (hg19) chr6:g.40354242C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354242C>T , CM000668.2:g.40354242C>T GRCh38
NC_000006.11:g.40321981C>T , CM000668.1:g.40321981C>T GRCh37
NC_000006.10:g.40429959C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1765G>A
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