Canonical Allele Identifier: CA706049026

Gene: LINC02302

Linked Data

• dbSNP Id: rs1224882377
• gnomAD v3: 14-44637438-GT-G
• gnomAD v4: 14-44637438-GT-G
• MyVariant Identifiers: chr14:g.45106642del (hg19) ; chr14:g.44637439del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44637440del , CM000676.2:g.44637440del	GRCh38
NC_000014.8:g.45106643del , CM000676.1:g.45106643del	GRCh37
NC_000014.7:g.44176393del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943800.1:n.226-40426del
XR_943801.1:n.226-40426del
XR_943806.1:n.226-40426del
XR_943808.1:n.126+160491del