Canonical Allele Identifier: CA754459776
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1281871943
gnomAD v3: 2-103961931-G-T
gnomAD v4: 2-103961931-G-T
MyVariant Identifiers: chr2:g.104578389G>T (hg19) chr2:g.103961931G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103961931G>T , CM000664.2:g.103961931G>T GRCh38
NC_000002.11:g.104578389G>T , CM000664.1:g.104578389G>T GRCh37
NC_000002.10:g.103944821G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739621.1:n.178+87486G>T
XR_001739623.1:n.178+87486G>T
Search 100 bp 5'
Search 100 bp 3'