HGVS | Genome Assembly |
---|---|
NC_000009.12:g.128945626G= , CM000671.2:g.128945626G= | GRCh38 |
NC_000009.11:g.131707905G= , CM000671.1:g.131707905G= | GRCh37 |
NC_000009.10:g.130747726G= | NCBI36 |
NG_017009.1:g.7108C= , LRG_744:g.7108C= | |
NG_033111.1:g.2934G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372586.4:c.*61C= MANE Select | ENSP00000361667.3:n.*61C= | |
ENST00000372586.3:c.*61C= | ENSP00000361667.3:n.*61C= | |
ENST00000482796.1:c.39-3563G= | ENSP00000417556.2:n.39-3563G= | |
NM_014908.3:c.*61C= , LRG_744t1:c.*61C= | NP_055723.1:n.*61C= | |
NM_014908.4:c.*61C= MANE Select | NP_055723.1:n.*61C= |