HGVS | Genome Assembly |
---|---|
NC_000023.11:g.116172675T>C , CM000685.2:g.116172675T>C | GRCh38 |
NC_000023.10:g.115303928T>C , CM000685.1:g.115303928T>C | GRCh37 |
NC_000023.9:g.115217956T>C | NCBI36 |
NG_016326.1:g.6971T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371906.5:c.395T>C MANE Select | ENSP00000360973.4:p.Ile132Thr | |
ENST00000680409.1:n.863T>C | ||
ENST00000681852.1:c.395T>C | ENSP00000505750.1:p.Ile132Thr | |
ENST00000371906.4:c.395T>C | ENSP00000360973.4:p.Ile132Thr | |
NM_000686.4:c.395T>C | NP_000677.2:p.Ile132Thr | |
XM_011537533.1:c.395T>C | XP_011535835.1:p.Ile132Thr | |
NM_000686.5:c.395T>C MANE Select | NP_000677.2:p.Ile132Thr | |
NM_001385624.1:c.395T>C | NP_001372553.1:p.Ile132Thr |