Canonical Allele Identifier: CA137815808
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1054438193
gnomAD v2: 6-40321933-G-T
gnomAD v3: 6-40354194-G-T
gnomAD v4: 6-40354194-G-T
MyVariant Identifiers: chr6:g.40321933G>T (hg19) chr6:g.40354194G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354194G>T , CM000668.2:g.40354194G>T GRCh38
NC_000006.11:g.40321933G>T , CM000668.1:g.40321933G>T GRCh37
NC_000006.10:g.40429911G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1813C>A
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Search 100 bp 3'