Canonical Allele Identifier: CA1889344553
Gene:

Linked Data

dbSNP Id: rs1832130723
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697639T>G , CM000672.2:g.8697639T>G GRCh38
NC_000010.10:g.8739602T>G , CM000672.1:g.8739602T>G GRCh37
NC_000010.9:g.8779608T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27838A>C
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