Canonical Allele Identifier: CA471213839
Gene: LINC01475 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101287588G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527831G>C , CM000672.2:g.99527831G>C GRCh38
NC_000010.10:g.101287588G>C , CM000672.1:g.101287588G>C GRCh37
NC_000010.9:g.101277578G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.552C>G
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