Canonical Allele Identifier: CA1332325128
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.226155869T= , CM000664.2:g.226155869T= GRCh38
NC_000002.11:g.227020585T= , CM000664.1:g.227020585T= GRCh37
NC_000002.10:g.226728829T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046102.1:n.293-8519T=