Canonical Allele Identifier: CA547127626

Gene: LINC02045

Linked Data

• dbSNP Id: rs1173720423
• gnomAD v2: 3-147935679-C-A
• gnomAD v3: 3-148217892-C-A
• gnomAD v4: 3-148217892-C-A
• MyVariant Identifiers: chr3:g.147935679C>A (hg19) ; chr3:g.148217892C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148217892C>A , CM000665.2:g.148217892C>A	GRCh38
NC_000003.11:g.147935679C>A , CM000665.1:g.147935679C>A	GRCh37
NC_000003.10:g.149418369C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_924565.1:n.86+2618G>T