Canonical Allele Identifier: CA2246165620
Gene:

Linked Data

dbSNP Id: rs1165715298
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137298T>A , CM000679.2:g.8137298T>A GRCh38
NC_000017.10:g.8040616T>A , CM000679.1:g.8040616T>A GRCh37
NC_000017.9:g.7981341T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1551T>A
XR_934203.1:n.70-2179T>A
XR_934202.2:n.414-1551T>A
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