Canonical Allele Identifier: CA903927137

Gene: LINC02043

Linked Data

• dbSNP Id: rs1301213235
• gnomAD v3: 3-186812691-CAT-C
• gnomAD v4: 3-186812691-CAT-C
• MyVariant Identifiers: chr3:g.186530481_186530482del (hg19) ; chr3:g.186812692_186812693del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186812692_186812693del , CM000665.2:g.186812692_186812693del	GRCh38
NC_000003.11:g.186530481_186530482del , CM000665.1:g.186530481_186530482del	GRCh37
NC_000003.10:g.188013175_188013176del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_125409.1:n.564-545_564-544del