Canonical Allele Identifier: CA824631306
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1309398808
MyVariant Identifiers: chr6:g.40321982T>C (hg19) chr6:g.40354243T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354243T>C , CM000668.2:g.40354243T>C GRCh38
NC_000006.11:g.40321982T>C , CM000668.1:g.40321982T>C GRCh37
NC_000006.10:g.40429960T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1764A>G
Search 100 bp 5'
Search 100 bp 3'