Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046623T= , CM000667.2:g.136046623T= | GRCh38 |
| NC_000005.9:g.135382312T= , CM000667.1:g.135382312T= | GRCh37 |
| NC_000005.8:g.135410211T= | NCBI36 |
| NG_012646.1:g.22729T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.459+128T= MANE Select | ENSP00000416330.2:n.459+128T= | |
| ENST00000442011.6:c.459+128T= | ENSP00000416330.2:n.459+128T= | |
| ENST00000506699.5:n.652T= | ||
| ENST00000507018.5:c.437+67T= | ||
| ENST00000515433.1:n.879T= | ||
| NM_000358.2:c.459+128T= | NP_000349.1:n.459+128T= | |
| NM_000358.3:c.459+128T= MANE Select | NP_000349.1:n.459+128T= |