Canonical Allele Identifier: CA709662668
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1338156549

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021419A>G , CM000676.2:g.88021419A>G GRCh38
NC_000014.8:g.88487763A>G , CM000676.1:g.88487763A>G GRCh37
NC_000014.7:g.87557516A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110121.1:n.327+2256T>C