Canonical Allele Identifier: CA2336565989
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41648211A= , CM000681.2:g.41648211A= GRCh38
NC_000019.9:g.42152132A= , CM000681.1:g.42152132A= GRCh37
NC_000019.8:g.46843972A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935972.1:n.170+3291T=