Canonical Allele Identifier: CA1034488299
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1680649735
gnomAD v3: 2-103962058-T-G
gnomAD v4: 2-103962058-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962058T>G , CM000664.2:g.103962058T>G GRCh38
NC_000002.11:g.104578516T>G , CM000664.1:g.104578516T>G GRCh37
NC_000002.10:g.103944948T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87613T>G
XR_001739623.1:n.178+87613T>G
Search 100 bp 5'
Search 100 bp 3'