Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6019315A= , CM000674.2:g.6019315A= | GRCh38 |
| NC_000012.11:g.6128481A= , CM000674.1:g.6128481A= | GRCh37 |
| NC_000012.10:g.5998742A= | NCBI36 |
| NG_009072.1:g.110356T= | |
| NG_009072.2:g.110356T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.4103T= MANE Select | ENSP00000261405.5:p.Ile1368= | |
| ENST00000261405.9:c.4103T= | ENSP00000261405.5:p.Ile1368= | |
| ENST00000538635.5:n.421-25381T= | ||
| NM_000552.3:c.4103T= | NP_000543.2:p.Ile1368= | |
| NM_000552.4:c.4103T= | NP_000543.2:p.Ile1368= | |
| NM_000552.5:c.4103T= MANE Select | NP_000543.3:p.Ile1368= |