HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154993077T>G , CM000685.2:g.154993077T>G | GRCh38 |
NC_000023.10:g.154221352T>G , CM000685.1:g.154221352T>G | GRCh37 |
NC_000023.9:g.153874546T>G | NCBI36 |
NG_011403.1:g.34647A>C | |
NG_011403.2:g.34647A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.460A>C MANE Select | ENSP00000353393.4:p.Thr154Pro | |
ENST00000647125.1:c.*246A>C | ENSP00000496062.1:n.*246A>C | |
ENST00000360256.8:c.460A>C | ENSP00000353393.4:p.Thr154Pro | |
ENST00000423959.5:c.355A>C | ENSP00000409446.1:p.Thr119Pro | |
ENST00000453950.1:c.442A>C | ENSP00000389153.1:p.Thr148Pro | |
NM_000132.3:c.460A>C | NP_000123.1:p.Thr154Pro | |
XM_011531126.1:c.355A>C | XP_011529428.1:p.Thr119Pro | |
NM_000132.4:c.460A>C MANE Select | NP_000123.1:p.Thr154Pro |