HGVS | Genome Assembly |
---|---|
NC_000001.11:g.161222388A= , CM000663.2:g.161222388A= | GRCh38 |
NC_000001.10:g.161192178A= , CM000663.1:g.161192178A= | GRCh37 |
NC_000001.9:g.159458802A= | NCBI36 |
NG_012043.1:g.6241T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367990.7:c.*17T= MANE Select | ENSP00000356969.3:n.*17T= | |
ENST00000463812.1:c.*17T= | ENSP00000476890.1:n.*17T= | |
ENST00000464492.5:c.*17T= | ENSP00000476911.1:n.*17T= | |
ENST00000468465.5:c.*17T= | ENSP00000476662.1:n.*17T= | |
ENST00000470459.6:c.*17T= | ENSP00000477031.1:n.*17T= | |
ENST00000481413.1:n.831T= | ||
ENST00000481511.5:c.*317T= | ENSP00000477054.1:n.*317T= | |
ENST00000491350.1:c.*103T= | ENSP00000477353.1:n.*103T= | |
NM_001643.1:c.*17T= | NP_001634.1:n.*17T= | |
NM_001643.2:c.*17T= MANE Select | NP_001634.1:n.*17T= |