Canonical Allele Identifier: CA1672979011
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633458T= , CM000668.2:g.151633458T= GRCh38
NC_000006.11:g.151954593T= , CM000668.1:g.151954593T= GRCh37
NC_000006.10:g.151996286T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3476T=