Canonical Allele Identifier: CA2391929895
Gene: LINC00163 HGNC NCBI

Linked Data

dbSNP Id: rs13046884

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44993730A>C , CM000683.2:g.44993730A>C GRCh38
NC_000021.8:g.46413645A>C , CM000683.1:g.46413645A>C GRCh37
NC_000021.7:g.45238073A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_033840.1:n.183+174T>G