Canonical Allele Identifier: CA1623081678
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762013264
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354007A>G , CM000668.2:g.40354007A>G GRCh38
NC_000006.11:g.40321746A>G , CM000668.1:g.40321746A>G GRCh37
NC_000006.10:g.40429724A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.2000T>C
Search 100 bp 5'
Search 100 bp 3'