Canonical Allele Identifier: CA471214385
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs1589970314
MyVariant Identifiers: chr10:g.101287775C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99528018C>G , CM000672.2:g.99528018C>G GRCh38
NC_000010.10:g.101287775C>G , CM000672.1:g.101287775C>G GRCh37
NC_000010.9:g.101277765C>G NCBI36
NG_016854.1:g.86C>G

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.365G>C