HGVS | Genome Assembly |
---|---|
NC_000015.10:g.45480160T= , CM000677.2:g.45480160T= | GRCh38 |
NC_000015.9:g.45772358T= , CM000677.1:g.45772358T= | GRCh37 |
NC_000015.8:g.43559650T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261867.5:c.*5003A= MANE Select | ENSP00000261867.3:n.*5003A= | |
ENST00000261867.4:c.*5003A= | ENSP00000261867.3:n.*5003A= | |
NM_013309.5:c.*5003A= | NP_037441.2:n.*5003A= | |
NM_013309.6:c.*5003A= MANE Select | NP_037441.2:n.*5003A= |