Canonical Allele Identifier: CA846958552

Gene: LINC02964

Linked Data

• dbSNP Id: rs1182862451
• MyVariant Identifiers: chr8:g.126539963A>C (hg19) ; chr8:g.125527721A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125527721A>C , CM000670.2:g.125527721A>C	GRCh38
NC_000008.10:g.126539963A>C , CM000670.1:g.126539963A>C	GRCh37
NC_000008.9:g.126609145A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_928628.1:n.256+54407A>C
XR_001746072.1:n.583+4708A>C
XR_001746073.1:n.583+4708A>C