Canonical Allele Identifier: CA89215089
Gene: LINC00578 HGNC NCBI

Linked Data

dbSNP Id: rs750072744
MyVariant Identifiers: chr3:g.177291606G>A (hg19) chr3:g.177573818G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.177573818G>A , CM000665.2:g.177573818G>A GRCh38
NC_000003.11:g.177291606G>A , CM000665.1:g.177291606G>A GRCh37
NC_000003.10:g.178774300G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_047568.1:n.289+34325G>A
XR_924737.1:n.114-2452C>T
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