HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94031111G>C , CM000663.2:g.94031111G>C | GRCh38 |
NC_000001.10:g.94496667G>C , CM000663.1:g.94496667G>C | GRCh37 |
NC_000001.9:g.94269255G>C | NCBI36 |
NG_009073.1:g.95039C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.4138C>G MANE Select | ENSP00000359245.3:p.Pro1380Ala | |
ENST00000370225.3:c.4138C>G | ENSP00000359245.3:p.Pro1380Ala | |
ENST00000536513.5:c.514C>G | ENSP00000439707.2:p.Pro172Ala | |
NM_000350.2:c.4138C>G | NP_000341.2:p.Pro1380Ala | |
NM_000350.3:c.4138C>G MANE Select | NP_000341.2:p.Pro1380Ala |