Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.1233952T= , CM000669.2:g.1233952T= | GRCh38 |
| NC_000007.13:g.1273588T= , CM000669.1:g.1273588T= | GRCh37 |
| NC_000007.12:g.1240114T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316333.9:c.450+257T= MANE Select | ENSP00000314480.8:n.450+257T= | |
| ENST00000316333.8:c.450+257T= | ENSP00000314480.8:n.450+257T= | |
| NM_001080461.1:c.450+257T= | NP_001073930.1:n.450+257T= | |
| NM_001080461.2:c.450+257T= | NP_001073930.1:n.450+257T= | |
| NM_001080461.3:c.450+257T= MANE Select | NP_001073930.1:n.450+257T= |