Canonical Allele Identifier: CA2733843439
Gene:

Linked Data

dbSNP Id: rs2144614076
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211830T>A , CM000679.2:g.50211830T>A GRCh38
NC_000017.10:g.48289191T>A , CM000679.1:g.48289191T>A GRCh37
NC_000017.9:g.45644190T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-2005T>A
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