HGVS | Genome Assembly |
---|---|
NC_000014.9:g.50937718A= , CM000676.2:g.50937718A= | GRCh38 |
NC_000014.8:g.51404436A= , CM000676.1:g.51404436A= | GRCh37 |
NC_000014.7:g.50474186A= | NCBI36 |
NG_012796.1:g.11813T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000216392.8:c.345+18T= MANE Select | ENSP00000216392.7:n.345+18T= | |
ENST00000216392.7:c.345+18T= | ENSP00000216392.7:n.345+18T= | |
ENST00000530336.2:n.412+18T= | ||
ENST00000532462.5:c.345+18T= | ENSP00000431657.1:n.345+18T= | |
ENST00000544180.6:c.244-2533T= | ENSP00000443787.1:n.244-2533T= | |
NM_001163940.1:c.244-2533T= | NP_001157412.1:n.244-2533T= | |
NM_002863.4:c.345+18T= | NP_002854.3:n.345+18T= | |
NM_002863.5:c.345+18T= MANE Select | NP_002854.3:n.345+18T= | |
NM_001163940.2:c.244-2533T= | NP_001157412.1:n.244-2533T= |