Canonical Allele Identifier: CA2055289519
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293198C= , CM000674.2:g.93293198C= GRCh38
NC_000012.11:g.93686974C= , CM000674.1:g.93686974C= GRCh37
NC_000012.10:g.92211105C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34829G=