Canonical Allele Identifier: CA1931372987
Gene: LINC01475 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99529086A= , CM000672.2:g.99529086A= GRCh38
NC_000010.10:g.101288843A= , CM000672.1:g.101288843A= GRCh37
NC_000010.9:g.101278833A= NCBI36
NG_016854.1:g.1154A=

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.167-402T=