HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25010277T>G , CM000685.2:g.25010277T>G | GRCh38 |
NC_000023.10:g.25028394T>G , CM000685.1:g.25028394T>G | GRCh37 |
NC_000023.9:g.24938315T>G | NCBI36 |
NG_008281.1:g.10672A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000379044.5:c.1102A>C MANE Select | ENSP00000368332.4:p.Thr368Pro | |
ENST00000379044.4:c.1102A>C | ENSP00000368332.4:p.Thr368Pro | |
NM_139058.2:c.1102A>C | NP_620689.1:p.Thr368Pro | |
NM_139058.3:c.1102A>C MANE Select | NP_620689.1:p.Thr368Pro |