Canonical Allele Identifier: CA265472395
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs899771235

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021180C>T , CM000676.2:g.88021180C>T GRCh38
NC_000014.8:g.88487524C>T , CM000676.1:g.88487524C>T GRCh37
NC_000014.7:g.87557277C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110121.1:n.328-2477G>A