Canonical Allele Identifier: CA900438643

Gene: LINC02045

Linked Data

• dbSNP Id: rs1362204112
• gnomAD v3: 3-148217844-T-C
• gnomAD v4: 3-148217844-T-C
• MyVariant Identifiers: chr3:g.147935631T>C (hg19) ; chr3:g.148217844T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148217844T>C , CM000665.2:g.148217844T>C	GRCh38
NC_000003.11:g.147935631T>C , CM000665.1:g.147935631T>C	GRCh37
NC_000003.10:g.149418321T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924565.1:n.86+2666A>G