Canonical Allele Identifier: CA1889449167
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.9011211A= , CM000672.2:g.9011211A= GRCh38
NC_000010.10:g.9053174A= , CM000672.1:g.9053174A= GRCh37
NC_000010.9:g.9093180A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.32+54152T=