Canonical Allele Identifier: CA1889344540
Gene:

Linked Data

dbSNP Id: rs1469783569
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697620C>G , CM000672.2:g.8697620C>G GRCh38
NC_000010.10:g.8739583C>G , CM000672.1:g.8739583C>G GRCh37
NC_000010.9:g.8779589C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27819G>C
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