Canonical Allele Identifier: CA1889449110
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.9011179A= , CM000672.2:g.9011179A= GRCh38
NC_000010.10:g.9053142A= , CM000672.1:g.9053142A= GRCh37
NC_000010.9:g.9093148A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.32+54184T=