Canonical Allele Identifier: CA31223072

Gene: LINC02819

Linked Data

• dbSNP Id: rs941152926
• gnomAD v2: 1-159453867-A-G
• gnomAD v3: 1-159484077-A-G
• gnomAD v4: 1-159484077-A-G
• MyVariant Identifiers: chr1:g.159453867A>G (hg19) ; chr1:g.159484077A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159484077A>G , CM000663.2:g.159484077A>G	GRCh38
NC_000001.10:g.159453867A>G , CM000663.1:g.159453867A>G	GRCh37
NC_000001.9:g.157720491A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922189.1:n.678+1093A>G
XR_922189.3:n.690+1093A>G