Canonical Allele Identifier: CA706049041

Gene: LINC02302

Linked Data

• dbSNP Id: rs1454938804
• gnomAD v3: 14-44637448-C-T
• gnomAD v4: 14-44637448-C-T
• MyVariant Identifiers: chr14:g.45106651C>T (hg19) ; chr14:g.44637448C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44637448C>T , CM000676.2:g.44637448C>T	GRCh38
NC_000014.8:g.45106651C>T , CM000676.1:g.45106651C>T	GRCh37
NC_000014.7:g.44176401C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943800.1:n.226-40435G>A
XR_943801.1:n.226-40435G>A
XR_943806.1:n.226-40435G>A
XR_943808.1:n.126+160482G>A