HGVS | Genome Assembly |
---|---|
NC_000009.12:g.114785462T= , CM000671.2:g.114785462T= | GRCh38 |
NC_000009.11:g.117547742T= , CM000671.1:g.117547742T= | GRCh37 |
NC_000009.10:g.116587563T= | NCBI36 |
NG_011488.2:g.25667A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374045.5:c.*4990A= MANE Select | ENSP00000363157.3:n.*4990A= | |
ENST00000374045.4:c.*4990A= | ENSP00000363157.3:n.*4990A= | |
NM_001204344.1:c.5569A= | NP_001191273.1:n.5569A= | |
NM_005118.3:c.*4990A= | NP_005109.2:n.*4990A= | |
NM_005118.4:c.*4990A= MANE Select | NP_005109.2:n.*4990A= |