Canonical Allele Identifier: CA2055289516
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293194T= , CM000674.2:g.93293194T= GRCh38
NC_000012.11:g.93686970T= , CM000674.1:g.93686970T= GRCh37
NC_000012.10:g.92211101T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34833A=