Canonical Allele Identifier: CA2730094311
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs2139789265

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021161A>G , CM000676.2:g.88021161A>G GRCh38
NC_000014.8:g.88487505A>G , CM000676.1:g.88487505A>G GRCh37
NC_000014.7:g.87557258A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.328-2458T>C