Canonical Allele Identifier: CA534753687

Gene: LINC01965

Linked Data

• dbSNP Id: rs1355947161
• gnomAD v2: 2-104578489-T-C
• gnomAD v3: 2-103962031-T-C
• gnomAD v4: 2-103962031-T-C
• MyVariant Identifiers: chr2:g.104578489T>C (hg19) ; chr2:g.103962031T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103962031T>C , CM000664.2:g.103962031T>C	GRCh38
NC_000002.11:g.104578489T>C , CM000664.1:g.104578489T>C	GRCh37
NC_000002.10:g.103944921T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001739621.1:n.178+87586T>C
XR_001739623.1:n.178+87586T>C