Canonical Allele Identifier: CA2153421343
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1595259227

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021222T>G , CM000676.2:g.88021222T>G GRCh38
NC_000014.8:g.88487566T>G , CM000676.1:g.88487566T>G GRCh37
NC_000014.7:g.87557319T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110121.1:n.327+2453A>C