Canonical Allele Identifier: CA13472498
Gene: LINC02744 HGNC NCBI

Linked Data

dbSNP Id: rs11217617
gnomAD v2: 11-119863505-C-T
gnomAD v3: 11-119992796-C-T
gnomAD v4: 11-119992796-C-T
MyVariant Identifiers: chr11:g.119863505C>T (hg19) chr11:g.119992796C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119992796C>T , CM000673.2:g.119992796C>T GRCh38
NC_000011.9:g.119863505C>T , CM000673.1:g.119863505C>T GRCh37
NC_000011.8:g.119368715C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948086.1:n.590G>A
XR_948087.1:n.199+1798G>A
XR_948088.1:n.77G>A
XR_948089.1:n.77G>A
XR_948090.1:n.176+1798G>A
XR_948091.1:n.177+1798G>A
XR_948092.1:n.77G>A
XR_948093.1:n.177+1798G>A
XR_948094.1:n.175+1798G>A
XR_948095.1:n.77G>A
XR_948096.1:n.174+1798G>A
XR_002957267.1:n.2129G>A
XR_948086.2:n.682G>A
XR_948087.2:n.346+1798G>A
XR_948088.3:n.2132G>A
XR_948089.3:n.2130G>A
XR_948090.2:n.338+1798G>A
XR_948091.2:n.340+1798G>A
XR_948092.3:n.2131G>A
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