HGVS | Genome Assembly |
---|---|
NC_000010.11:g.16937656C>T , CM000672.2:g.16937656C>T | GRCh38 |
NC_000010.10:g.16979655C>T , CM000672.1:g.16979655C>T | GRCh37 |
NC_000010.9:g.17019661C>T | NCBI36 |
NG_008967.1:g.197162G>A , LRG_540:g.197162G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377833.10:c.5862G>A MANE Select | ENSP00000367064.4:p.Lys1954= | |
ENST00000377833.8:c.5862G>A | ENSP00000367064.4:p.Lys1954= | |
NM_001081.3:c.5862G>A , LRG_540t1:c.5862G>A | NP_001072.2:p.Lys1954= | |
XM_011519708.1:c.5862G>A | XP_011518010.1:p.Lys1954= | |
XM_011519709.1:c.1848G>A | XP_011518011.1:p.Lys616= | |
XM_011519710.1:c.1824G>A | XP_011518012.1:p.Lys608= | |
XM_011519711.1:c.1704G>A | XP_011518013.1:p.Lys568= | |
XM_011519708.2:c.5862G>A | XP_011518010.1:p.Lys1954= | |
XM_011519709.2:c.1848G>A | XP_011518011.1:p.Lys616= | |
XM_011519710.2:c.1824G>A | XP_011518012.1:p.Lys608= | |
XM_011519711.3:c.1704G>A | XP_011518013.1:p.Lys568= | |
NM_001081.4:c.5862G>A MANE Select | NP_001072.2:p.Lys1954= |