Canonical Allele Identifier: CA85231827

Gene: LINC02045

Linked Data

• dbSNP Id: rs1004063766
• gnomAD v3: 3-148217748-G-A
• gnomAD v4: 3-148217748-G-A
• MyVariant Identifiers: chr3:g.147935535G>A (hg19) ; chr3:g.148217748G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148217748G>A , CM000665.2:g.148217748G>A	GRCh38
NC_000003.11:g.147935535G>A , CM000665.1:g.147935535G>A	GRCh37
NC_000003.10:g.149418225G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924565.1:n.86+2762C>T