Canonical Allele Identifier: CA1704517759
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46032926G= , CM000669.2:g.46032926G= GRCh38
NC_000007.13:g.46072524G= , CM000669.1:g.46072524G= GRCh37
NC_000007.12:g.46039049G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745203.1:n.1270-3692G=