Canonical Allele Identifier: CA773444779
Gene:

Linked Data

dbSNP Id: rs1257525055
MyVariant Identifiers: chr17:g.55866213G>A (hg19) chr17:g.57788852G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788852G>A , CM000679.2:g.57788852G>A GRCh38
NC_000017.10:g.55866213G>A , CM000679.1:g.55866213G>A GRCh37
NC_000017.9:g.53221212G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16656C>T
XR_934881.3:n.3815-16656C>T
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