Canonical Allele Identifier: CA1905920017
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318644T= , CM000672.2:g.43318644T= GRCh38
NC_000010.10:g.43814092T= , CM000672.1:g.43814092T= GRCh37
NC_000010.9:g.43134098T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945902.1:n.108+49T=
XR_945902.2:n.198+49T=