Canonical Allele Identifier: CA222002623
Gene:

Linked Data

dbSNP Id: rs775347214
gnomAD v3: 11-45506559-G-A
gnomAD v4: 11-45506559-G-A
MyVariant Identifiers: chr11:g.45528109G>A (hg19) chr11:g.45506559G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506559G>A , CM000673.2:g.45506559G>A GRCh38
NC_000011.9:g.45528109G>A , CM000673.1:g.45528109G>A GRCh37
NC_000011.8:g.45484685G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16788C>T
XR_931245.3:n.566-16788C>T
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