HGVS | Genome Assembly |
---|---|
NC_000009.12:g.92718840G= , CM000671.2:g.92718840G= | GRCh38 |
NC_000009.11:g.95481122G= , CM000671.1:g.95481122G= | GRCh37 |
NC_000009.10:g.94520943G= | NCBI36 |
NG_033908.1:g.50962C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356884.11:c.1805C= MANE Select | ENSP00000349351.6:p.Thr602= | |
ENST00000356884.10:c.1805C= | ENSP00000349351.6:p.Thr602= | |
ENST00000375512.3:c.1805C= | ENSP00000364662.3:p.Thr602= | |
NM_001003800.1:c.1805C= | NP_001003800.1:p.Thr602= | |
NM_015250.3:c.1805C= | NP_056065.1:p.Thr602= | |
XM_017014551.1:c.1886C= | XP_016870040.1:p.Thr629= | |
NM_001003800.2:c.1805C= MANE Select | NP_001003800.1:p.Thr602= | |
NM_015250.4:c.1805C= | NP_056065.1:p.Thr602= |