HGVS | Genome Assembly |
---|---|
NC_000015.10:g.71811786T>C , CM000677.2:g.71811786T>C | GRCh38 |
NC_000015.9:g.72104126T>C , CM000677.1:g.72104126T>C | GRCh37 |
NC_000015.8:g.69891180T>C | NCBI36 |
NG_009113.2:g.6232T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000617575.5:c.266T>C MANE Select | ENSP00000482504.1:p.Met89Thr | |
ENST00000617575.4:c.266T>C | ENSP00000482504.1:p.Met89Thr | |
ENST00000621098.1:c.266T>C | ENSP00000479962.1:p.Met89Thr | |
ENST00000621736.4:c.2T>C | ENSP00000479254.1:p.Met1Thr | |
NM_014249.3:c.266T>C | NP_055064.1:p.Met89Thr | |
NM_016346.3:c.266T>C | NP_057430.1:p.Met89Thr | |
XM_011521146.1:c.2T>C | XP_011519448.1:p.Met1Thr | |
NM_014249.4:c.266T>C MANE Select | NP_055064.1:p.Met89Thr | |
NM_016346.4:c.266T>C | NP_057430.1:p.Met89Thr |