Canonical Allele Identifier: CA86469753

Gene: LINC00880

Linked Data

• dbSNP Id: rs940492485
• MyVariant Identifiers: chr3:g.156837109T>C (hg19) ; chr3:g.157119320T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.157119320T>C , CM000665.2:g.157119320T>C	GRCh38
NC_000003.11:g.156837109T>C , CM000665.1:g.156837109T>C	GRCh37
NC_000003.10:g.158319803T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_034007.1:n.127+3556A>G