Canonical Allele Identifier: CA2141801201
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.62501707C= , CM000676.2:g.62501707C= GRCh38
NC_000014.8:g.62968425C= , CM000676.1:g.62968425C= GRCh37
NC_000014.7:g.62038178C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943932.1:n.116-2334C=
XR_943932.2:n.103-2334C=