Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.18672032G>C , CM000685.2:g.18672032G>C | GRCh38 |
| NC_000023.10:g.18690152G>C , CM000685.1:g.18690152G>C | GRCh37 |
| NC_000023.9:g.18600073G>C | NCBI36 |
| NG_008659.3:g.10417C>G , LRG_702:g.10417C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379984.4:c.37C>G MANE Select | ENSP00000369320.3:p.Leu13Val | |
| ENST00000379984.3:c.37C>G | ENSP00000369320.3:p.Leu13Val | |
| NM_000330.3:c.37C>G , LRG_702t1:c.37C>G | NP_000321.1:p.Leu13Val | |
| NM_000330.4:c.37C>G MANE Select | NP_000321.1:p.Leu13Val |