Canonical Allele Identifier: CA602397097
Gene: LINC02744 HGNC NCBI

Linked Data

dbSNP Id: rs1378929969
gnomAD v2: 11-119863629-A-G
gnomAD v3: 11-119992920-A-G
gnomAD v4: 11-119992920-A-G
MyVariant Identifiers: chr11:g.119863629A>G (hg19) chr11:g.119992920A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119992920A>G , CM000673.2:g.119992920A>G GRCh38
NC_000011.9:g.119863629A>G , CM000673.1:g.119863629A>G GRCh37
NC_000011.8:g.119368839A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948086.1:n.466T>C
XR_948087.1:n.199+1674T>C
XR_948090.1:n.176+1674T>C
XR_948091.1:n.177+1674T>C
XR_948093.1:n.177+1674T>C
XR_948094.1:n.175+1674T>C
XR_948096.1:n.174+1674T>C
XR_002957267.1:n.2005T>C
XR_948086.2:n.558T>C
XR_948087.2:n.346+1674T>C
XR_948088.3:n.2008T>C
XR_948089.3:n.2006T>C
XR_948090.2:n.338+1674T>C
XR_948091.2:n.340+1674T>C
XR_948092.3:n.2007T>C
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