Canonical Allele Identifier: CA89215083
Gene: LINC00578 HGNC NCBI

Linked Data

dbSNP Id: rs956347252
gnomAD v3: 3-177573811-G-A
gnomAD v4: 3-177573811-G-A
MyVariant Identifiers: chr3:g.177291599G>A (hg19) chr3:g.177573811G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.177573811G>A , CM000665.2:g.177573811G>A GRCh38
NC_000003.11:g.177291599G>A , CM000665.1:g.177291599G>A GRCh37
NC_000003.10:g.178774293G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_047568.1:n.289+34318G>A
XR_924737.1:n.114-2445C>T
Search 100 bp 5'
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