HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20778583T= , CM000686.2:g.20778583T= | GRCh38 |
NC_000024.9:g.22940469T= , CM000686.1:g.22940469T= | GRCh37 |
NC_000024.8:g.21349857T= | NCBI36 |
NG_032924.1:g.27516T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000629237.2:c.533-926T= MANE Select | ENSP00000486252.1:n.533-926T= | |
ENST00000629237.1:c.533-926T= | ENSP00000486252.1:n.533-926T= | |
NM_001039567.2:c.533-926T= | NP_001034656.1:n.533-926T= | |
XM_011531423.1:c.482-926T= | XP_011529725.1:n.482-926T= | |
NM_001039567.3:c.533-926T= MANE Select | NP_001034656.1:n.533-926T= |