HGVS | Genome Assembly |
---|---|
NC_000014.9:g.21312461A>C , CM000676.2:g.21312461A>C | GRCh38 |
NC_000014.8:g.21780620A>C , CM000676.1:g.21780620A>C | GRCh37 |
NC_000014.7:g.20850460A>C | NCBI36 |
NG_008933.1:g.29485A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000400017.7:c.1106A>C MANE Select | ENSP00000382895.2:p.Lys369Thr | |
ENST00000400017.6:c.1106A>C | ENSP00000382895.2:p.Lys369Thr | |
ENST00000556336.5:c.1025A>C | ENSP00000450445.1:p.Lys342Thr | |
ENST00000557771.5:c.1025A>C | ENSP00000451219.1:p.Lys342Thr | |
NM_020366.3:c.1106A>C | NP_065099.3:p.Lys369Thr | |
XM_011536983.1:c.1073A>C | XP_011535285.1:p.Lys358Thr | |
NM_020366.4:c.1106A>C MANE Select | NP_065099.3:p.Lys369Thr |