HGVS | Genome Assembly |
---|---|
NC_000007.14:g.120664989T= , CM000669.2:g.120664989T= | GRCh38 |
NC_000007.13:g.120305043T= , CM000669.1:g.120305043T= | GRCh37 |
NC_000007.12:g.120092279T= | NCBI36 |
NG_034230.1:g.396322T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331113.9:c.1116-67914T= MANE Select | ENSP00000333496.4:n.1116-67914T= | |
ENST00000331113.8:c.1116-67914T= | ENSP00000333496.4:n.1116-67914T= | |
NM_012281.2:c.1116-67914T= | NP_036413.1:n.1116-67914T= | |
NM_012281.3:c.1116-67914T= MANE Select | NP_036413.1:n.1116-67914T= |