Canonical Allele Identifier: CA53064911
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1041578839
MyVariant Identifiers: chr2:g.104578596G>T (hg19) chr2:g.103962138G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962138G>T , CM000664.2:g.103962138G>T GRCh38
NC_000002.11:g.104578596G>T , CM000664.1:g.104578596G>T GRCh37
NC_000002.10:g.103945028G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87693G>T
XR_001739623.1:n.178+87693G>T
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Search 100 bp 3'