Canonical Allele Identifier: CA1609069973
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525249T= , CM000668.2:g.8525249T= GRCh38
NC_000006.11:g.8525482T= , CM000668.1:g.8525482T= GRCh37
NC_000006.10:g.8470481T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038979.1:n.626-33336T=
NR_038980.1:n.649-33336T=