Canonical Allele Identifier: CA706049031

Gene: LINC02302

Linked Data

• dbSNP Id: rs1379090571
• gnomAD v3: 14-44637441-C-T
• gnomAD v4: 14-44637441-C-T
• MyVariant Identifiers: chr14:g.45106644C>T (hg19) ; chr14:g.44637441C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44637441C>T , CM000676.2:g.44637441C>T	GRCh38
NC_000014.8:g.45106644C>T , CM000676.1:g.45106644C>T	GRCh37
NC_000014.7:g.44176394C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943800.1:n.226-40428G>A
XR_943801.1:n.226-40428G>A
XR_943806.1:n.226-40428G>A
XR_943808.1:n.126+160489G>A