Canonical Allele Identifier: CA219833908
Gene:

Linked Data

dbSNP Id: rs1026860792
gnomAD v2: 11-27505673-T-C
gnomAD v3: 11-27484126-T-C
gnomAD v4: 11-27484126-T-C
MyVariant Identifiers: chr11:g.27505673T>C (hg19) chr11:g.27484126T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484126T>C , CM000673.2:g.27484126T>C GRCh38
NC_000011.9:g.27505673T>C , CM000673.1:g.27505673T>C GRCh37
NC_000011.8:g.27462249T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.277T>C
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