HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128300906G= , CM000667.2:g.128300906G= | GRCh38 |
NC_000005.9:g.127636598G= , CM000667.1:g.127636598G= | GRCh37 |
NC_000005.8:g.127664497G= | NCBI36 |
NG_008750.1:g.242138C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000703783.1:n.2861C= | ||
ENST00000703785.1:n.2780C= | ||
ENST00000262464.9:c.6077C= MANE Select | ENSP00000262464.4:p.Ser2026= | |
ENST00000262464.8:c.6077C= | ENSP00000262464.4:p.Ser2026= | |
ENST00000508053.5:c.6077C= | ENSP00000424571.1:p.Ser2026= | |
ENST00000619499.4:c.6074C= | ENSP00000482132.1:p.Ser2025= | |
NM_001999.3:c.6077C= | NP_001990.2:p.Ser2026= | |
XM_017009228.2:c.5924C= | XP_016864717.1:p.Ser1975= | |
NM_001999.4:c.6077C= MANE Select | NP_001990.2:p.Ser2026= |