Canonical Allele Identifier: CA2055289526
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293220A= , CM000674.2:g.93293220A= GRCh38
NC_000012.11:g.93686996A= , CM000674.1:g.93686996A= GRCh37
NC_000012.10:g.92211127A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34807T=