Canonical Allele Identifier: CA706049092

Gene: LINC02302

Linked Data

• dbSNP Id: rs1248771249
• MyVariant Identifiers: chr14:g.45106762C>T (hg19) ; chr14:g.44637559C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44637559C>T , CM000676.2:g.44637559C>T	GRCh38
NC_000014.8:g.45106762C>T , CM000676.1:g.45106762C>T	GRCh37
NC_000014.7:g.44176512C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943800.1:n.226-40546G>A
XR_943801.1:n.226-40546G>A
XR_943806.1:n.226-40546G>A
XR_943808.1:n.126+160371G>A