Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240877152T= , CM000664.2:g.240877152T= | GRCh38 |
| NC_000002.11:g.241816569T= , CM000664.1:g.241816569T= | GRCh37 |
| NC_000002.10:g.241465242T= | NCBI36 |
| NG_008005.1:g.13408T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.847-385T= MANE Select | ENSP00000302620.3:n.847-385T= | |
| ENST00000307503.3:c.847-385T= | ENSP00000302620.3:n.847-385T= | |
| ENST00000470255.1:n.240T= | ||
| NM_000030.2:c.847-385T= | NP_000021.1:n.847-385T= | |
| NM_000030.3:c.847-385T= MANE Select | NP_000021.1:n.847-385T= |