Canonical Allele Identifier: CA534753689
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1258873858
gnomAD v2: 2-104578527-C-A
gnomAD v3: 2-103962069-C-A
gnomAD v4: 2-103962069-C-A
MyVariant Identifiers: chr2:g.104578527C>A (hg19) chr2:g.103962069C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962069C>A , CM000664.2:g.103962069C>A GRCh38
NC_000002.11:g.104578527C>A , CM000664.1:g.104578527C>A GRCh37
NC_000002.10:g.103944959C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87624C>A
XR_001739623.1:n.178+87624C>A
Search 100 bp 5'
Search 100 bp 3'