Canonical Allele Identifier: CA1422921591
Gene: LINC00578 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.177573813G= , CM000665.2:g.177573813G= GRCh38
NC_000003.11:g.177291601G= , CM000665.1:g.177291601G= GRCh37
NC_000003.10:g.178774295G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_047568.1:n.289+34320G=
XR_924737.1:n.114-2447C=