Canonical Allele Identifier: CA1899276918
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30230903C= , CM000672.2:g.30230903C= GRCh38
NC_000010.10:g.30519832C= , CM000672.1:g.30519832C= GRCh37
NC_000010.9:g.30559838C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120653.1:n.269-14C=