Canonical Allele Identifier: CA900438591

Gene: LINC02045

Linked Data

• dbSNP Id: rs12496119
• gnomAD v3: 3-148217631-C-T
• gnomAD v4: 3-148217631-C-T
• MyVariant Identifiers: chr3:g.147935418C>T (hg19) ; chr3:g.148217631C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148217631C>T , CM000665.2:g.148217631C>T	GRCh38
NC_000003.11:g.147935418C>T , CM000665.1:g.147935418C>T	GRCh37
NC_000003.10:g.149418108C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924565.1:n.86+2879G>A