Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184060059A= , CM000665.2:g.184060059A= | GRCh38 |
| NC_000003.11:g.183777847A= , CM000665.1:g.183777847A= | GRCh37 |
| NC_000003.10:g.185260541A= | NCBI36 |
| NG_012749.1:g.12013A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318351.2:c.1141+16A= MANE Select | ENSP00000322617.1:n.1141+16A= | |
| ENST00000318351.1:c.1141+16A= | ENSP00000322617.1:n.1141+16A= | |
| NM_130770.2:c.1141+16A= | NP_570126.2:n.1141+16A= | |
| NM_130770.3:c.1141+16A= MANE Select | NP_570126.2:n.1141+16A= |