Canonical Allele Identifier: CA2141801229
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.62501725G= , CM000676.2:g.62501725G= GRCh38
NC_000014.8:g.62968443G= , CM000676.1:g.62968443G= GRCh37
NC_000014.7:g.62038196G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943932.1:n.116-2316G=
XR_943932.2:n.103-2316G=