Canonical Allele Identifier: CA313629862
Gene:

Linked Data

dbSNP Id: rs908889231
MyVariant Identifiers: chr20:g.23642510G>C (hg19) chr20:g.23661873G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661873G>C , CM000682.2:g.23661873G>C GRCh38
NC_000020.10:g.23642510G>C , CM000682.1:g.23642510G>C GRCh37
NC_000020.9:g.23590510G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+223G>C
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