Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869122T= , CM000664.2:g.240869122T= | GRCh38 |
| NC_000002.11:g.241808539T= , CM000664.1:g.241808539T= | GRCh37 |
| NC_000002.10:g.241457212T= | NCBI36 |
| NG_008005.1:g.5378T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.166-48T= MANE Select | ENSP00000302620.3:n.166-48T= | |
| ENST00000307503.3:c.166-48T= | ENSP00000302620.3:n.166-48T= | |
| ENST00000472436.1:n.186-48T= | ||
| NM_000030.2:c.166-48T= | NP_000021.1:n.166-48T= | |
| XR_924060.1:n.405+1111A= | ||
| NM_000030.3:c.166-48T= MANE Select | NP_000021.1:n.166-48T= |