Canonical Allele Identifier: CA1674885869
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812625T= , CM000668.2:g.155812625T= GRCh38
NC_000006.11:g.156133759T= , CM000668.1:g.156133759T= GRCh37
NC_000006.10:g.156175451T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19206T=
XR_943146.1:n.645-586A=
XR_001744423.1:n.699-586A=
XR_001744424.1:n.79+19206T=