Canonical Allele Identifier: CA2711319442
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs2113771122
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354255C>A , CM000668.2:g.40354255C>A GRCh38
NC_000006.11:g.40321994C>A , CM000668.1:g.40321994C>A GRCh37
NC_000006.10:g.40429972C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1752G>T
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Search 100 bp 3'