Canonical Allele Identifier: CA53064916
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs935055235
gnomAD v3: 2-103962151-A-G
gnomAD v4: 2-103962151-A-G
MyVariant Identifiers: chr2:g.104578609A>G (hg19) chr2:g.103962151A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962151A>G , CM000664.2:g.103962151A>G GRCh38
NC_000002.11:g.104578609A>G , CM000664.1:g.104578609A>G GRCh37
NC_000002.10:g.103945041A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87706A>G
XR_001739623.1:n.178+87706A>G
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