HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111098331C= , CM000667.2:g.111098331C= | GRCh38 |
NC_000005.9:g.110434029C= , CM000667.1:g.110434029C= | GRCh37 |
NC_000005.8:g.110461928C= | NCBI36 |
NG_008979.1:g.11160C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000513710.4:c.292-391C= MANE Select | ENSP00000424628.3:n.292-391C= | |
ENST00000504122.2:n.174-391C= | ||
ENST00000505303.5:n.428-391C= | ||
ENST00000506538.6:c.460-391C= | ENSP00000423067.2:n.460-391C= | |
ENST00000513710.3:c.292-391C= | ENSP00000424628.3:n.292-391C= | |
ENST00000612402.4:c.460-391C= | ENSP00000479950.1:n.460-391C= | |
NM_139281.2:c.460-391C= | NP_644810.1:n.460-391C= | |
XM_011543163.1:c.460-391C= | XP_011541465.1:n.460-391C= | |
NM_139281.3:c.292-391C= MANE Select | NP_644810.2:n.292-391C= |