Canonical Allele Identifier: CA473651107
Gene:

Linked Data

dbSNP Id: rs897101406
gnomAD v3: 11-27484083-C-G
gnomAD v4: 11-27484083-C-G
MyVariant Identifiers: chr11:g.27505630C>G (hg19) chr11:g.27484083C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484083C>G , CM000673.2:g.27484083C>G GRCh38
NC_000011.9:g.27505630C>G , CM000673.1:g.27505630C>G GRCh37
NC_000011.8:g.27462206C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.234C>G
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