Canonical Allele Identifier: CA773444785
Gene:

Linked Data

dbSNP Id: rs935321186
MyVariant Identifiers: chr17:g.55866233C>G (hg19) chr17:g.57788872C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788872C>G , CM000679.2:g.57788872C>G GRCh38
NC_000017.10:g.55866233C>G , CM000679.1:g.55866233C>G GRCh37
NC_000017.9:g.53221232C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16676G>C
XR_934881.3:n.3815-16676G>C
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