Canonical Allele Identifier: CA289293275
Gene:

Linked Data

dbSNP Id: rs950606774
MyVariant Identifiers: chr17:g.28564151G>T (hg19) chr17:g.30237133G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237133G>T , CM000679.2:g.30237133G>T GRCh38
NC_000017.10:g.28564151G>T , CM000679.1:g.28564151G>T GRCh37
NC_000017.9:g.25588277G>T NCBI36
NG_011747.2:g.3804C>A

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+63G>T
XR_001752824.1:n.280+63G>T
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