Canonical Allele Identifier: CA2469672207
Gene: LINC00278 HGNC NCBI

Linked Data

dbSNP Id: rs1603312990
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.3004612G>T , CM000686.2:g.3004612G>T GRCh38
NC_000024.9:g.2872653G>T , CM000686.1:g.2872653G>T GRCh37
NC_000024.8:g.2932653G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046502.1:n.222+1395G>T
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