Canonical Allele Identifier: CA2153421396
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1595259271

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021263A>C , CM000676.2:g.88021263A>C GRCh38
NC_000014.8:g.88487607A>C , CM000676.1:g.88487607A>C GRCh37
NC_000014.7:g.87557360A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2412T>G