Canonical Allele Identifier: CA901232180

Gene: LINC00880

Linked Data

• dbSNP Id: rs1160873336
• MyVariant Identifiers: chr3:g.156836942C>G (hg19) ; chr3:g.157119153C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.157119153C>G , CM000665.2:g.157119153C>G	GRCh38
NC_000003.11:g.156836942C>G , CM000665.1:g.156836942C>G	GRCh37
NC_000003.10:g.158319636C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_034007.1:n.127+3723G>C