Canonical Allele Identifier: CA900438597

Gene: LINC02045

Linked Data

• dbSNP Id: rs1343042657
• MyVariant Identifiers: chr3:g.147935433T>C (hg19) ; chr3:g.148217646T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148217646T>C , CM000665.2:g.148217646T>C	GRCh38
NC_000003.11:g.147935433T>C , CM000665.1:g.147935433T>C	GRCh37
NC_000003.10:g.149418123T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924565.1:n.86+2864A>G