Canonical Allele Identifier: CA1905919962
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318520G= , CM000672.2:g.43318520G= GRCh38
NC_000010.10:g.43813968G= , CM000672.1:g.43813968G= GRCh37
NC_000010.9:g.43133974G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945902.1:n.33G=
XR_945902.2:n.123G=