Canonical Allele Identifier: CA290054835
Gene:

Linked Data

dbSNP Id: rs890492399
MyVariant Identifiers: chr17:g.35880804T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880804T>A , CM000679.2:g.35880804T>A GRCh38
NC_000017.9:g.31231921T>A NCBI36
NG_015990.1:g.4570A>T

Transcript Alleles

HGVS Amino-acid Change
XR_934696.1:n.197-3578T>A
XR_934697.1:n.200-3578T>A
XR_001752852.1:n.426+730T>A
XR_934696.2:n.91-3578T>A
XR_934697.2:n.91-3578T>A
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