Canonical Allele Identifier: CA14744687
Gene: LINC01535 HGNC NCBI

Linked Data

dbSNP Id: rs7246657

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.37256206T>C , CM000681.2:g.37256206T>C GRCh38
NC_000019.9:g.37747108T>C , CM000681.1:g.37747108T>C GRCh37
NC_000019.8:g.42438948T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110718.1:n.383-193T>C
NR_110719.1:n.382+224T>C
NR_110720.1:n.383+224T>C
NR_110720.2:n.356+224T>C