HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111098197G= , CM000667.2:g.111098197G= | GRCh38 |
NC_000005.9:g.110433895G= , CM000667.1:g.110433895G= | GRCh37 |
NC_000005.8:g.110461794G= | NCBI36 |
NG_008979.1:g.11026G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000513710.4:c.292-525G= MANE Select | ENSP00000424628.3:n.292-525G= | |
ENST00000504122.2:n.174-525G= | ||
ENST00000505303.5:n.428-525G= | ||
ENST00000506538.6:c.460-525G= | ENSP00000423067.2:n.460-525G= | |
ENST00000513710.3:c.292-525G= | ENSP00000424628.3:n.292-525G= | |
ENST00000612402.4:c.460-525G= | ENSP00000479950.1:n.460-525G= | |
NM_139281.2:c.460-525G= | NP_644810.1:n.460-525G= | |
XM_011543163.1:c.460-525G= | XP_011541465.1:n.460-525G= | |
NM_139281.3:c.292-525G= MANE Select | NP_644810.2:n.292-525G= |