MyVariant.info:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21033518_21033519dup , CM000664.2:g.21033518_21033519dup | GRCh38 |
| NC_000002.11:g.21256390_21256391dup , CM000664.1:g.21256390_21256391dup | GRCh37 |
| NC_000002.10:g.21109895_21109896dup | NCBI36 |
| NG_011793.1:g.15555_15556dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673739.2:c.*211-1_*211dup | ||
| ENST00000673882.2:c.*211-1_*211dup | ||
| ENST00000673739.1:c.619-1_619dup | ||
| ENST00000673882.1:c.619-1_619dup | ||
| ENST00000233242.5:c.905-1_905dup | ||
| ENST00000399256.4:c.905-1_905dup | ||
| ENST00000616098.4:c.905-1_905dup | ||
| NM_000384.2:c.905-1_905dup | ||
| XM_011532809.1:c.905-1_905dup | ||
| NM_000384.3:c.905-1_905dup |