Canonical Allele Identifier: CA222002630
Gene:

Linked Data

dbSNP Id: rs927509973
gnomAD v2: 11-45528177-G-A
gnomAD v3: 11-45506627-G-A
gnomAD v4: 11-45506627-G-A
MyVariant Identifiers: chr11:g.45528177G>A (hg19) chr11:g.45506627G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506627G>A , CM000673.2:g.45506627G>A GRCh38
NC_000011.9:g.45528177G>A , CM000673.1:g.45528177G>A GRCh37
NC_000011.8:g.45484753G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16856C>T
XR_931245.3:n.566-16856C>T
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