Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202377323G= , CM000664.2:g.202377323G= | GRCh38 |
| NC_000002.11:g.203242046G= , CM000664.1:g.203242046G= | GRCh37 |
| NC_000002.10:g.202950291G= | NCBI36 |
| NG_009363.1:g.5997G= , LRG_712:g.5997G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.-152G= MANE Select | ENSP00000363708.4:n.-152G= | |
| ENST00000374580.8:c.-152G= | ENSP00000363708.4:n.-152G= | |
| NM_001204.6:c.-152G= , LRG_712t1:c.-152G= | NP_001195.2:n.-152G= | |
| XM_011511687.1:c.-152G= | XP_011509989.1:n.-152G= | |
| XM_011511688.1:c.-152G= | XP_011509990.1:n.-152G= | |
| NM_001204.7:c.-152G= MANE Select | NP_001195.2:n.-152G= |