Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1394324A= , CM000667.2:g.1394324A= | GRCh38 |
| NC_000005.9:g.1394439A= , CM000667.1:g.1394439A= | GRCh37 |
| NC_000005.8:g.1447439A= | NCBI36 |
| NG_015885.1:g.56105T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000270349.12:c.*411T= MANE Select | ENSP00000270349.9:n.*411T= | |
| ENST00000270349.11:c.*411T= | ENSP00000270349.9:n.*411T= | |
| ENST00000512002.2:n.655T= | ||
| NM_001044.4:c.*411T= | NP_001035.1:n.*411T= | |
| NM_001044.5:c.*411T= MANE Select | NP_001035.1:n.*411T= |