Canonical Allele Identifier: CA137815798
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs747772433
MyVariant Identifiers: chr6:g.40321822C>T (hg19) chr6:g.40354083C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354083C>T , CM000668.2:g.40354083C>T GRCh38
NC_000006.11:g.40321822C>T , CM000668.1:g.40321822C>T GRCh37
NC_000006.10:g.40429800C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1924G>A
Search 100 bp 5'
Search 100 bp 3'