Canonical Allele Identifier: CA761543497
Gene: LINC01934 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.181131318A>C , CM000664.2:g.181131318A>C GRCh38
NC_000002.11:g.181996045A>C , CM000664.1:g.181996045A>C GRCh37
NC_000002.10:g.181704290A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130784.1:n.144+7338A>C