Canonical Allele Identifier: CA615660995
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1276483372

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021302G>C , CM000676.2:g.88021302G>C GRCh38
NC_000014.8:g.88487646G>C , CM000676.1:g.88487646G>C GRCh37
NC_000014.7:g.87557399G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2373C>G