Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869123T= , CM000664.2:g.240869123T= | GRCh38 |
| NC_000002.11:g.241808540T= , CM000664.1:g.241808540T= | GRCh37 |
| NC_000002.10:g.241457213T= | NCBI36 |
| NG_008005.1:g.5379T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.166-47T= MANE Select | ENSP00000302620.3:n.166-47T= | |
| ENST00000307503.3:c.166-47T= | ENSP00000302620.3:n.166-47T= | |
| ENST00000472436.1:n.186-47T= | ||
| NM_000030.2:c.166-47T= | NP_000021.1:n.166-47T= | |
| XR_924060.1:n.405+1110A= | ||
| NM_000030.3:c.166-47T= MANE Select | NP_000021.1:n.166-47T= |