Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31861067T= , CM000668.2:g.31861067T= | GRCh38 |
| NC_000006.11:g.31828844T= , CM000668.1:g.31828844T= | GRCh37 |
| NC_000006.10:g.31936823T= | NCBI36 |
| NG_008201.1:g.6866A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375631.5:c.615+121A= MANE Select | ENSP00000364782.4:n.615+121A= | |
| ENST00000677054.1:n.1413A= | ||
| ENST00000677512.1:n.723+121A= | ||
| ENST00000678869.1:n.844A= | ||
| ENST00000375631.4:c.615+121A= | ENSP00000364782.4:n.615+121A= | |
| ENST00000480384.1:n.644+121A= | ||
| ENST00000491768.5:c.615+121A= | ENSP00000433127.1:n.615+121A= | |
| ENST00000495807.1:n.1304A= | ||
| NM_000434.3:c.615+121A= | NP_000425.1:n.615+121A= | |
| NM_000434.4:c.615+121A= MANE Select | NP_000425.1:n.615+121A= |