HGVS | Genome Assembly |
---|---|
NC_000008.11:g.22786183A= , CM000670.2:g.22786183A= | GRCh38 |
NC_000008.10:g.22643696A= , CM000670.1:g.22643696A= | GRCh37 |
NC_000008.9:g.22699641A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256404.8:c.357+31454T= MANE Select | ENSP00000256404.6:n.357+31454T= | |
ENST00000256404.7:c.357+31454T= | ENSP00000256404.6:n.357+31454T= | |
NM_144962.2:c.357+31454T= | NP_659399.2:n.357+31454T= | |
XM_011544413.1:c.357+31454T= | XP_011542715.1:n.357+31454T= | |
XM_011544414.1:c.357+31454T= | XP_011542716.1:n.357+31454T= | |
NM_001363233.1:c.357+31454T= | NP_001350162.1:n.357+31454T= | |
NM_144962.3:c.357+31454T= MANE Select | NP_659399.2:n.357+31454T= | |
NM_001363233.2:c.357+31454T= | NP_001350162.1:n.357+31454T= |