Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.18672031A>G , CM000685.2:g.18672031A>G | GRCh38 |
| NC_000023.10:g.18690151A>G , CM000685.1:g.18690151A>G | GRCh37 |
| NC_000023.9:g.18600072A>G | NCBI36 |
| NG_008659.3:g.10418T>C , LRG_702:g.10418T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000330.4:c.38T>C MANE Select | NP_000321.1:p.Leu13Pro |
| ENST00000379984.4:c.38T>C MANE Select | ENSP00000369320.3:p.Leu13Pro |
| NM_000330.3:c.38T>C , LRG_702t1:c.38T>C | NP_000321.1:p.Leu13Pro |
| ENST00000379984.3:c.38T>C | ENSP00000369320.3:p.Leu13Pro |