Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31348741A>G , CM000664.2:g.31348741A>G | GRCh38 |
| NC_000002.11:g.31571607A>G , CM000664.1:g.31571607A>G | GRCh37 |
| NC_000002.10:g.31425111A>G | NCBI36 |
| NG_008871.1:g.71005T>C | |
| NG_008871.2:g.71005T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379416.4:c.3051+158T>C MANE Select | ENSP00000368727.3:n.3051+158T>C | |
| ENST00000379416.3:c.3051+158T>C | ENSP00000368727.3:n.3051+158T>C | |
| NM_000379.3:c.3051+158T>C | NP_000370.2:n.3051+158T>C | |
| XM_011533095.1:c.3048+158T>C | XP_011531397.1:n.3048+158T>C | |
| XM_011533096.1:c.3051+158T>C | XP_011531398.1:n.3051+158T>C | |
| XM_011533095.2:c.3048+158T>C | XP_011531397.1:n.3048+158T>C | |
| XM_011533096.2:c.3051+158T>C | XP_011531398.1:n.3051+158T>C | |
| NM_000379.4:c.3051+158T>C MANE Select | NP_000370.2:n.3051+158T>C |