Canonical Allele Identifier: CA566857037
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1354146530
gnomAD v2: 6-40321730-A-C
gnomAD v3: 6-40353991-A-C
gnomAD v4: 6-40353991-A-C
MyVariant Identifiers: chr6:g.40321730A>C (hg19) chr6:g.40353991A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353991A>C , CM000668.2:g.40353991A>C GRCh38
NC_000006.11:g.40321730A>C , CM000668.1:g.40321730A>C GRCh37
NC_000006.10:g.40429708A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.2016T>G
Search 100 bp 5'
Search 100 bp 3'