Canonical Allele Identifier: CA224770960
Gene: LINC02757 HGNC NCBI

Linked Data

dbSNP Id: rs376774804
gnomAD v3: 11-76621175-T-C
gnomAD v4: 11-76621175-T-C
MyVariant Identifiers: chr11:g.76332219T>C (hg19) chr11:g.76621175T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.76621175T>C , CM000673.2:g.76621175T>C GRCh38
NC_000011.9:g.76332219T>C , CM000673.1:g.76332219T>C GRCh37
NC_000011.8:g.76009867T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247265.2:n.2147+4693A>G
XR_950334.1:n.2082+5398A>G
XR_001748311.1:n.2245+4693A>G
XR_001748312.1:n.1515+4693A>G
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