Canonical Allele Identifier: CA1818149112
Gene:

Linked Data

dbSNP Id: rs1814932635
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999229C>G , CM000670.2:g.126999229C>G GRCh38
NC_000008.10:g.128011474C>G , CM000670.1:g.128011474C>G GRCh37
NC_000008.9:g.128080656C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1301-7326C>G
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