Canonical Allele Identifier: CA89215101

Gene: LINC00578

Linked Data

• dbSNP Id: rs567447516
• gnomAD v3: 3-177573868-C-T
• gnomAD v4: 3-177573868-C-T
• MyVariant Identifiers: chr3:g.177291656C>T (hg19) ; chr3:g.177573868C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.177573868C>T , CM000665.2:g.177573868C>T	GRCh38
NC_000003.11:g.177291656C>T , CM000665.1:g.177291656C>T	GRCh37
NC_000003.10:g.178774350C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_047568.1:n.289+34375C>T
XR_924737.1:n.114-2502G>A