HGVS | Genome Assembly |
---|---|
NC_000008.11:g.22786124C= , CM000670.2:g.22786124C= | GRCh38 |
NC_000008.10:g.22643637C= , CM000670.1:g.22643637C= | GRCh37 |
NC_000008.9:g.22699582C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256404.8:c.357+31513G= MANE Select | ENSP00000256404.6:n.357+31513G= | |
ENST00000256404.7:c.357+31513G= | ENSP00000256404.6:n.357+31513G= | |
NM_144962.2:c.357+31513G= | NP_659399.2:n.357+31513G= | |
XM_011544413.1:c.357+31513G= | XP_011542715.1:n.357+31513G= | |
XM_011544414.1:c.357+31513G= | XP_011542716.1:n.357+31513G= | |
NM_001363233.1:c.357+31513G= | NP_001350162.1:n.357+31513G= | |
NM_144962.3:c.357+31513G= MANE Select | NP_659399.2:n.357+31513G= | |
NM_001363233.2:c.357+31513G= | NP_001350162.1:n.357+31513G= |