Canonical Allele Identifier: CA260254665

Gene: LINC02302

Linked Data

• dbSNP Id: rs145295500
• gnomAD v2: 14-45106599-C-G
• gnomAD v3: 14-44637396-C-G
• gnomAD v4: 14-44637396-C-G
• MyVariant Identifiers: chr14:g.45106599C>G (hg19) ; chr14:g.44637396C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44637396C>G , CM000676.2:g.44637396C>G	GRCh38
NC_000014.8:g.45106599C>G , CM000676.1:g.45106599C>G	GRCh37
NC_000014.7:g.44176349C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943800.1:n.226-40383G>C
XR_943801.1:n.226-40383G>C
XR_943806.1:n.226-40383G>C
XR_943808.1:n.126+160534G>C