Canonical Allele Identifier: CA287548676
Gene:

Linked Data

dbSNP Id: rs868138929
MyVariant Identifiers: chr17:g.8041138G>C (hg19) chr17:g.8137820G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137820G>C , CM000679.2:g.8137820G>C GRCh38
NC_000017.10:g.8041138G>C , CM000679.1:g.8041138G>C GRCh37
NC_000017.9:g.7981863G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1029G>C
XR_934203.1:n.70-1657G>C
XR_934202.2:n.414-1029G>C
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