Canonical Allele Identifier: CA1623081774
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762015594
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354206C>T , CM000668.2:g.40354206C>T GRCh38
NC_000006.11:g.40321945C>T , CM000668.1:g.40321945C>T GRCh37
NC_000006.10:g.40429923C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1801G>A
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Search 100 bp 3'