Canonical Allele Identifier: CA824631278
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1438425758
MyVariant Identifiers: chr6:g.40321919T>C (hg19) chr6:g.40354180T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354180T>C , CM000668.2:g.40354180T>C GRCh38
NC_000006.11:g.40321919T>C , CM000668.1:g.40321919T>C GRCh37
NC_000006.10:g.40429897T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1827A>G
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