Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160540105T= , CM000668.2:g.160540105T= | GRCh38 |
| NC_000006.11:g.160961137T= , CM000668.1:g.160961137T= | GRCh37 |
| NC_000006.10:g.160881127T= | NCBI36 |
| NG_016147.1:g.131271A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005577.4:c.5673A= MANE Select | NP_005568.2:p.Ile1891= |
| ENST00000316300.10:c.5673A= MANE Select | ENSP00000321334.6:p.Ile1891= |
| NM_005577.2:c.5673A= | NP_005568.2:p.Ile1891= |
| NM_005577.3:c.5673A= | NP_005568.2:p.Ile1891= |
| ENST00000316300.9:c.5673A= | ENSP00000321334.5:p.Ile1891= |