HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44286541T= , CM000683.2:g.44286541T= | GRCh38 |
NC_000021.8:g.45706424T= , CM000683.1:g.45706424T= | GRCh37 |
NC_000021.7:g.44530852T= | NCBI36 |
NG_009556.1:g.5662T= , LRG_18:g.5662T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291582.6:c.133-16T= MANE Select | ENSP00000291582.5:n.133-16T= | |
ENST00000291582.5:c.133-16T= | ENSP00000291582.5:n.133-16T= | |
ENST00000527919.5:n.294-16T= | ||
ENST00000530812.5:n.302-16T= | ||
NM_000383.3:c.133-16T= | NP_000374.1:n.133-16T= | |
XM_011529551.1:c.133-16T= | XP_011527853.1:n.133-16T= | |
NM_000383.4:c.133-16T= MANE Select | NP_000374.1:n.133-16T= |