Canonical Allele Identifier: CA1931373000
Gene: LINC01475 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99529091C= , CM000672.2:g.99529091C= GRCh38
NC_000010.10:g.101288848C= , CM000672.1:g.101288848C= GRCh37
NC_000010.9:g.101278838C= NCBI36
NG_016854.1:g.1159C=

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.167-407G=