Canonical Allele Identifier: CA292624997
Gene:

Linked Data

dbSNP Id: rs372280426
MyVariant Identifiers: chr17:g.55866152A>G (hg19) chr17:g.57788791A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788791A>G , CM000679.2:g.57788791A>G GRCh38
NC_000017.10:g.55866152A>G , CM000679.1:g.55866152A>G GRCh37
NC_000017.9:g.53221151A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934881.1:n.1608-16595T>C
XR_934881.3:n.3815-16595T>C
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