Canonical Allele Identifier: CA38657584
Gene:

Linked Data

dbSNP Id: rs1857246
MyVariant Identifiers: chr1:g.224256223C>G (hg19) chr1:g.224068521C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068521C>G , CM000663.2:g.224068521C>G GRCh38
NC_000001.10:g.224256223C>G , CM000663.1:g.224256223C>G GRCh37
NC_000001.9:g.222322846C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949173.1:n.385+867C>G
XR_001737824.1:n.242+867C>G
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