Canonical Allele Identifier: CA824631311
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1353366121
gnomAD v3: 6-40354263-G-A
gnomAD v4: 6-40354263-G-A
MyVariant Identifiers: chr6:g.40322002G>A (hg19) chr6:g.40354263G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354263G>A , CM000668.2:g.40354263G>A GRCh38
NC_000006.11:g.40322002G>A , CM000668.1:g.40322002G>A GRCh37
NC_000006.10:g.40429980G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1744C>T
Search 100 bp 5'
Search 100 bp 3'