Canonical Allele Identifier: CA1056770959

Gene: LINC00578

Linked Data

• dbSNP Id: rs1717721293
• gnomAD v3: 3-177573948-C-T
• gnomAD v4: 3-177573948-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.177573948C>T , CM000665.2:g.177573948C>T	GRCh38
NC_000003.11:g.177291736C>T , CM000665.1:g.177291736C>T	GRCh37
NC_000003.10:g.178774430C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_047568.1:n.289+34455C>T
XR_924737.1:n.114-2582G>A