Canonical Allele Identifier: CA566857045
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs577641647
gnomAD v2: 6-40321829-T-G
MyVariant Identifiers: chr6:g.40321829T>G (hg19) chr6:g.40354090T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354090T>G , CM000668.2:g.40354090T>G GRCh38
NC_000006.11:g.40321829T>G , CM000668.1:g.40321829T>G GRCh37
NC_000006.10:g.40429807T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1917A>C
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