Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.20579842T= , CM000686.2:g.20579842T= | GRCh38 |
| NC_000024.9:g.22741728T= , CM000686.1:g.22741728T= | GRCh37 |
| NC_000024.8:g.21151116T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361365.7:c.100+151T= MANE Select | ENSP00000354722.2:n.100+151T= | |
| ENST00000361365.6:c.100+151T= | ENSP00000354722.2:n.100+151T= | |
| ENST00000382772.3:c.100+151T= | ENSP00000372222.3:n.100+151T= | |
| ENST00000465253.1:n.194+151T= | ||
| NM_001278612.1:c.100+151T= | NP_001265541.1:n.100+151T= | |
| NM_004681.3:c.100+151T= | NP_004672.2:n.100+151T= | |
| NM_004681.4:c.100+151T= MANE Select | NP_004672.2:n.100+151T= | |
| NM_001278612.2:c.100+151T= | NP_001265541.1:n.100+151T= |