Canonical Allele Identifier: CA137815814
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1028107798
MyVariant Identifiers: chr6:g.40321989T>A (hg19) chr6:g.40354250T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354250T>A , CM000668.2:g.40354250T>A GRCh38
NC_000006.11:g.40321989T>A , CM000668.1:g.40321989T>A GRCh37
NC_000006.10:g.40429967T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1757A>T
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