Canonical Allele Identifier: CA2153421322
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1339452502

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021203C>T , CM000676.2:g.88021203C>T GRCh38
NC_000014.8:g.88487547C>T , CM000676.1:g.88487547C>T GRCh37
NC_000014.7:g.87557300C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2472G>A