Canonical Allele Identifier: CA31223123

Gene: LINC02819

Linked Data

• dbSNP Id: rs779163694
• gnomAD v3: 1-159484226-AT-A
• gnomAD v4: 1-159484226-AT-A
• MyVariant Identifiers: chr1:g.159454017del (hg19) ; chr1:g.159484227del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159484228del , CM000663.2:g.159484228del	GRCh38
NC_000001.10:g.159454018del , CM000663.1:g.159454018del	GRCh37
NC_000001.9:g.157720642del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922189.1:n.678+1244del
XR_922189.3:n.690+1244del