Canonical Allele Identifier: CA85231863

Gene: LINC02045

Linked Data

• dbSNP Id: rs767535633
• gnomAD v2: 3-147935665-T-C
• gnomAD v3: 3-148217878-T-C
• gnomAD v4: 3-148217878-T-C
• MyVariant Identifiers: chr3:g.147935665T>C (hg19) ; chr3:g.148217878T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148217878T>C , CM000665.2:g.148217878T>C	GRCh38
NC_000003.11:g.147935665T>C , CM000665.1:g.147935665T>C	GRCh37
NC_000003.10:g.149418355T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924565.1:n.86+2632A>G