Canonical Allele Identifier: CA219833909
Gene:

Linked Data

dbSNP Id: rs1027567744
gnomAD v4: 11-27484127-A-G
MyVariant Identifiers: chr11:g.27505674A>G (hg19) chr11:g.27484127A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484127A>G , CM000673.2:g.27484127A>G GRCh38
NC_000011.9:g.27505674A>G , CM000673.1:g.27505674A>G GRCh37
NC_000011.8:g.27462250A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.278A>G
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