Canonical Allele Identifier: CA89215100

Gene: LINC00578

Linked Data

• dbSNP Id: rs922078786
• gnomAD v2: 3-177291640-T-G
• gnomAD v3: 3-177573852-T-G
• gnomAD v4: 3-177573852-T-G
• MyVariant Identifiers: chr3:g.177291640T>G (hg19) ; chr3:g.177573852T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.177573852T>G , CM000665.2:g.177573852T>G	GRCh38
NC_000003.11:g.177291640T>G , CM000665.1:g.177291640T>G	GRCh37
NC_000003.10:g.178774334T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_047568.1:n.289+34359T>G
XR_924737.1:n.114-2486A>C