Canonical Allele Identifier: CA14677488
Community Standard Title: NC_000019.10:g.47867845C>T
Gene: LINC01595 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47867845C>T , CM000681.2:g.47867845C>T GRCh38
NC_000019.9:g.48371102C>T , CM000681.1:g.48371102C>T GRCh37
NC_000019.8:g.53062914C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936005.1:n.320+1195G>A
XR_936005.2:n.322+1195G>A
XR_936006.1:n.320+1195G>A
XR_936006.2:n.322+1195G>A