Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15540362T= , CM000681.2:g.15540362T= | GRCh38 |
| NC_000019.9:g.15651173T= , CM000681.1:g.15651173T= | GRCh37 |
| NC_000019.8:g.15512173T= | NCBI36 |
| NG_007987.1:g.36838T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269703.8:c.672-88T= MANE Select | ENSP00000269703.1:n.672-88T= | |
| ENST00000269703.7:c.672-88T= | ENSP00000269703.1:n.672-88T= | |
| ENST00000601005.2:c.672-88T= | ENSP00000469866.1:n.672-88T= | |
| NM_173483.3:c.672-88T= | NP_775754.2:n.672-88T= | |
| XM_011527692.1:c.672-88T= | XP_011525994.1:n.672-88T= | |
| XM_011527693.1:c.672-88T= | XP_011525995.1:n.672-88T= | |
| XM_011527692.2:c.672-88T= | XP_011525994.1:n.672-88T= | |
| XM_011527693.2:c.672-88T= | XP_011525995.1:n.672-88T= | |
| NM_173483.4:c.672-88T= MANE Select | NP_775754.2:n.672-88T= |