Canonical Allele Identifier: CA2008287926
Gene:

Linked Data

dbSNP Id: rs1943912085
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128870951A>G , CM000673.2:g.128870951A>G GRCh38
NC_000011.9:g.128740846A>G , CM000673.1:g.128740846A>G GRCh37
NC_000011.8:g.128246056A>G NCBI36
NG_009379.1:g.1423T>C

Transcript Alleles

HGVS Amino-acid Change
XR_948172.1:n.5960T>C
XR_948173.1:n.5649T>C
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