Canonical Allele Identifier: CA600319190
Gene: LINC02757 HGNC NCBI

Linked Data

dbSNP Id: rs1166681265
gnomAD v2: 11-76332250-T-C
gnomAD v3: 11-76621206-T-C
gnomAD v4: 11-76621206-T-C
MyVariant Identifiers: chr11:g.76332250T>C (hg19) chr11:g.76621206T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.76621206T>C , CM000673.2:g.76621206T>C GRCh38
NC_000011.9:g.76332250T>C , CM000673.1:g.76332250T>C GRCh37
NC_000011.8:g.76009898T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247265.2:n.2147+4662A>G
XR_950334.1:n.2082+5367A>G
XR_001748311.1:n.2245+4662A>G
XR_001748312.1:n.1515+4662A>G
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