Canonical Allele Identifier: CA547365203

Gene: LINC00880

Linked Data

• dbSNP Id: rs1476065683
• gnomAD v2: 3-156836945-A-C
• gnomAD v3: 3-157119156-A-C
• gnomAD v4: 3-157119156-A-C
• MyVariant Identifiers: chr3:g.156836945A>C (hg19) ; chr3:g.157119156A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.157119156A>C , CM000665.2:g.157119156A>C	GRCh38
NC_000003.11:g.156836945A>C , CM000665.1:g.156836945A>C	GRCh37
NC_000003.10:g.158319639A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_034007.1:n.127+3720T>G