Canonical Allele Identifier: CA680387008
Gene: LINC02757 HGNC NCBI

Linked Data

dbSNP Id: rs1254685721
MyVariant Identifiers: chr11:g.76332255C>G (hg19) chr11:g.76621211C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.76621211C>G , CM000673.2:g.76621211C>G GRCh38
NC_000011.9:g.76332255C>G , CM000673.1:g.76332255C>G GRCh37
NC_000011.8:g.76009903C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247265.2:n.2147+4657G>C
XR_950334.1:n.2082+5362G>C
XR_001748311.1:n.2245+4657G>C
XR_001748312.1:n.1515+4657G>C
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