HGVS | Genome Assembly |
---|---|
NC_000014.9:g.105529800C= , CM000676.2:g.105529800C= | GRCh38 |
NC_000014.8:g.105996137C= , CM000676.1:g.105996137C= | GRCh37 |
NC_000014.7:g.105067182C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000392519.7:c.*6C= MANE Select | ENSP00000376304.2:n.*6C= | |
ENST00000392519.6:c.*6C= | ENSP00000376304.2:n.*6C= | |
ENST00000431372.1:c.*6C= | ENSP00000407456.1:n.*6C= | |
NM_025268.2:c.*6C= | NP_079544.1:n.*6C= | |
XM_005268101.2:c.*6C= | XP_005268158.1:n.*6C= | |
XM_006720261.2:c.*6C= | XP_006720324.1:n.*6C= | |
XM_011537185.1:c.*6C= | XP_011535487.1:n.*6C= | |
XM_011537186.1:c.*6C= | XP_011535488.1:n.*6C= | |
NM_001331238.1:c.*6C= | NP_001318167.1:n.*6C= | |
NM_025268.3:c.*6C= | NP_079544.1:n.*6C= | |
XM_006720261.3:c.*6C= | XP_006720324.1:n.*6C= | |
NM_025268.4:c.*6C= MANE Select | NP_079544.1:n.*6C= | |
NM_001331238.2:c.*6C= | NP_001318167.1:n.*6C= |