Canonical Allele Identifier: CA11586308
Gene: LINC00886 HGNC NCBI

Linked Data

dbSNP Id: rs13068223

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.156753166A>G , CM000665.2:g.156753166A>G GRCh38
NC_000003.11:g.156470955A>G , CM000665.1:g.156470955A>G GRCh37
NC_000003.10:g.157953649A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038387.1:n.177-1983T>C