Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.185969149A= , CM000665.2:g.185969149A= | GRCh38 |
| NC_000003.11:g.185686938A= , CM000665.1:g.185686938A= | GRCh37 |
| NC_000003.10:g.187169632A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306399.3:n.270+441A= | ||
| ENST00000416764.5:n.349+432A= | ||
| ENST00000422108.5:n.288+500A= | ||
| ENST00000423298.5:n.137-2466A= | ||
| ENST00000436375.5:n.342+441A= | ||
| ENST00000445507.1:n.279+500A= | ||
| NR_033752.2:n.349+432A= | ||
| NR_151491.1:n.137-2466A= |