Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202464846T= , CM000664.2:g.202464846T= | GRCh38 |
| NC_000002.11:g.203329569T= , CM000664.1:g.203329569T= | GRCh37 |
| NC_000002.10:g.203037814T= | NCBI36 |
| NG_009363.1:g.93520T= , LRG_712:g.93520T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.114T= MANE Select | ENSP00000363708.4:p.Asp38= | |
| ENST00000638587.1:c.39T= | ENSP00000491062.1:p.Asp13= | |
| ENST00000374574.2:c.114T= | ENSP00000363702.2:p.Asp38= | |
| ENST00000374580.8:c.114T= | ENSP00000363708.4:p.Asp38= | |
| ENST00000479069.1:n.21T= | ||
| NM_001204.6:c.114T= , LRG_712t1:c.114T= | NP_001195.2:p.Asp38= | |
| XM_011511687.1:c.114T= | XP_011509989.1:p.Asp38= | |
| XM_011511688.1:c.114T= | XP_011509990.1:p.Asp38= | |
| NM_001204.7:c.114T= MANE Select | NP_001195.2:p.Asp38= |