Canonical Allele Identifier: CA219833904
Gene:

Linked Data

dbSNP Id: rs890133314
gnomAD v4: 11-27484100-G-A
MyVariant Identifiers: chr11:g.27505647G>A (hg19) chr11:g.27484100G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484100G>A , CM000673.2:g.27484100G>A GRCh38
NC_000011.9:g.27505647G>A , CM000673.1:g.27505647G>A GRCh37
NC_000011.8:g.27462223G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.251G>A
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