Canonical Allele Identifier: CA676911695
Gene:

Linked Data

dbSNP Id: rs1184238338
MyVariant Identifiers: chr11:g.45528189T>C (hg19) chr11:g.45506639T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506639T>C , CM000673.2:g.45506639T>C GRCh38
NC_000011.9:g.45528189T>C , CM000673.1:g.45528189T>C GRCh37
NC_000011.8:g.45484765T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16868A>G
XR_931245.3:n.566-16868A>G
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