Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6034741A= , CM000674.2:g.6034741A= | GRCh38 |
| NC_000012.11:g.6143907A= , CM000674.1:g.6143907A= | GRCh37 |
| NC_000012.10:g.6014168A= | NCBI36 |
| NG_009072.1:g.94930T= | |
| NG_009072.2:g.94930T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.2632T= MANE Select | ENSP00000261405.5:p.Phe878= | |
| ENST00000261405.9:c.2632T= | ENSP00000261405.5:p.Phe878= | |
| ENST00000538635.5:n.421-40807T= | ||
| NM_000552.3:c.2632T= | NP_000543.2:p.Phe878= | |
| NM_000552.4:c.2632T= | NP_000543.2:p.Phe878= | |
| NM_000552.5:c.2632T= MANE Select | NP_000543.3:p.Phe878= |