HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21007402T= , CM000664.2:g.21007402T= | GRCh38 |
NC_000002.11:g.21230274T= , CM000664.1:g.21230274T= | GRCh37 |
NC_000002.10:g.21083779T= | NCBI36 |
NG_011793.1:g.41672A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000233242.5:c.9466A= MANE Select | ENSP00000233242.1:p.Thr3156= | |
ENST00000616098.4:c.9466A= | ENSP00000477990.1:p.Thr3156= | |
NM_000384.2:c.9466A= | NP_000375.2:p.Thr3156= | |
XM_011532809.1:c.5869+3331A= | XP_011531111.1:n.5869+3331A= | |
NM_000384.3:c.9466A= MANE Select | NP_000375.3:p.Thr3156= |