Canonical Allele Identifier: CA2339623791
Community Standard Title: NC_000019.10:g.47868938C=
Gene: LINC01595 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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