Canonical Allele Identifier: CA2711319268
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs2113770899
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353922A>T , CM000668.2:g.40353922A>T GRCh38
NC_000006.11:g.40321661A>T , CM000668.1:g.40321661A>T GRCh37
NC_000006.10:g.40429639A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.2085T>A
Search 100 bp 5'
Search 100 bp 3'