Canonical Allele Identifier: CA15214264
Gene: LINC01173 HGNC NCBI
COSMIC:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.234706553A>C , CM000664.2:g.234706553A>C GRCh38
NC_000002.11:g.235615197A>C , CM000664.1:g.235615197A>C GRCh37
NC_000002.10:g.235279936A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_132376.1:n.201+10805A>C