Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202377327T= , CM000664.2:g.202377327T= | GRCh38 |
| NC_000002.11:g.203242050T= , CM000664.1:g.203242050T= | GRCh37 |
| NC_000002.10:g.202950295T= | NCBI36 |
| NG_009363.1:g.6001T= , LRG_712:g.6001T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.-148T= MANE Select | ENSP00000363708.4:n.-148T= | |
| ENST00000374580.8:c.-148T= | ENSP00000363708.4:n.-148T= | |
| NM_001204.6:c.-148T= , LRG_712t1:c.-148T= | NP_001195.2:n.-148T= | |
| XM_011511687.1:c.-148T= | XP_011509989.1:n.-148T= | |
| XM_011511688.1:c.-148T= | XP_011509990.1:n.-148T= | |
| NM_001204.7:c.-148T= MANE Select | NP_001195.2:n.-148T= |