Canonical Allele Identifier: CA2141801121
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.62501613A= , CM000676.2:g.62501613A= GRCh38
NC_000014.8:g.62968331A= , CM000676.1:g.62968331A= GRCh37
NC_000014.7:g.62038084A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943932.1:n.116-2428A=
XR_943932.2:n.103-2428A=