Canonical Allele Identifier: CA680386997
Gene: LINC02757 HGNC NCBI

Linked Data

dbSNP Id: rs1204444593
MyVariant Identifiers: chr11:g.76332243G>A (hg19) chr11:g.76621199G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.76621199G>A , CM000673.2:g.76621199G>A GRCh38
NC_000011.9:g.76332243G>A , CM000673.1:g.76332243G>A GRCh37
NC_000011.8:g.76009891G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247265.2:n.2147+4669C>T
XR_950334.1:n.2082+5374C>T
XR_001748311.1:n.2245+4669C>T
XR_001748312.1:n.1515+4669C>T
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