Canonical Allele Identifier: CA547127605

Gene: LINC02045

Linked Data

• dbSNP Id: rs959843857
• gnomAD v2: 3-147935425-G-C
• gnomAD v3: 3-148217638-G-C
• gnomAD v4: 3-148217638-G-C
• MyVariant Identifiers: chr3:g.147935425G>C (hg19) ; chr3:g.148217638G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148217638G>C , CM000665.2:g.148217638G>C	GRCh38
NC_000003.11:g.147935425G>C , CM000665.1:g.147935425G>C	GRCh37
NC_000003.10:g.149418115G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924565.1:n.86+2872C>G