Canonical Allele Identifier: CA1889449114
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.9011181T= , CM000672.2:g.9011181T= GRCh38
NC_000010.10:g.9053144T= , CM000672.1:g.9053144T= GRCh37
NC_000010.9:g.9093150T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.32+54182A=