Canonical Allele Identifier: CA2339623792
Gene: LINC01595 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47868938C>G , CM000681.2:g.47868938C>G GRCh38
NC_000019.9:g.48372195C>G , CM000681.1:g.48372195C>G GRCh37
NC_000019.8:g.53064007C>G NCBI36
NG_016745.1:g.22460G>C

Transcript Alleles

HGVS Amino-acid Change
XR_936005.1:n.320+102G>C
XR_936006.1:n.320+102G>C
XR_936005.2:n.322+102G>C
XR_936006.2:n.322+102G>C