Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.42353947C>G , CM000681.2:g.42353947C>G | GRCh38 |
| NC_000019.9:g.42858099C>G , CM000681.1:g.42858099C>G | GRCh37 |
| NC_000019.8:g.47549939C>G | NCBI36 |
| NG_033030.1:g.33339C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001271938.2:c.3934C>G MANE Select | NP_001258867.1:p.Leu1312Val |
| ENST00000251268.11:c.3934C>G MANE Select | ENSP00000251268.5:p.Leu1312Val |
| NM_001271938.1:c.3934C>G | NP_001258867.1:p.Leu1312Val |
| NM_001410.2:c.3733C>G | NP_001401.2:p.Leu1245Val |
| NM_001410.3:c.3733C>G | NP_001401.2:p.Leu1245Val |
| ENST00000251268.10:c.3934C>G | ENSP00000251268.5:p.Leu1312Val |
| ENST00000334370.8:c.3733C>G | ENSP00000334219.4:p.Leu1245Val |
| ENST00000378073.5:c.-3152C>G | ENSP00000367313.4:n.-3152C>G |