Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202530967A= , CM000664.2:g.202530967A= | GRCh38 |
| NC_000002.11:g.203395690A= , CM000664.1:g.203395690A= | GRCh37 |
| NC_000002.10:g.203103935A= | NCBI36 |
| NG_009363.1:g.159641A= , LRG_712:g.159641A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.1128+13A= MANE Select | ENSP00000363708.4:n.1128+13A= | |
| ENST00000638587.1:c.1059+13A= | ENSP00000491062.1:n.1059+13A= | |
| ENST00000374574.2:c.1128+13A= | ENSP00000363702.2:n.1128+13A= | |
| ENST00000374580.8:c.1128+13A= | ENSP00000363708.4:n.1128+13A= | |
| NM_001204.6:c.1128+13A= , LRG_712t1:c.1128+13A= | NP_001195.2:n.1128+13A= | |
| XM_011511687.1:c.1128+13A= | XP_011509989.1:n.1128+13A= | |
| XM_011511688.1:c.1128+13A= | XP_011509990.1:n.1128+13A= | |
| NM_001204.7:c.1128+13A= MANE Select | NP_001195.2:n.1128+13A= |