Canonical Allele Identifier: CA2136398952
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50857088C= , CM000676.2:g.50857088C= GRCh38
NC_000014.8:g.51323806C= , CM000676.1:g.51323806C= GRCh37
NC_000014.7:g.50393556C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1010G=
XR_943848.2:n.643+1010G=