Canonical Allele Identifier: CA1609069929
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525127T= , CM000668.2:g.8525127T= GRCh38
NC_000006.11:g.8525360T= , CM000668.1:g.8525360T= GRCh37
NC_000006.10:g.8470359T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038979.1:n.626-33458T=
NR_038980.1:n.649-33458T=