Canonical Allele Identifier: CA1905919972
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318545A= , CM000672.2:g.43318545A= GRCh38
NC_000010.10:g.43813993A= , CM000672.1:g.43813993A= GRCh37
NC_000010.9:g.43133999A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945902.1:n.58A=
XR_945902.2:n.148A=