HGVS | Genome Assembly |
---|---|
NC_000006.12:g.6145112T= , CM000668.2:g.6145112T= | GRCh38 |
NC_000006.11:g.6145345T= , CM000668.1:g.6145345T= | GRCh37 |
NC_000006.10:g.6090344T= | NCBI36 |
NG_008107.1:g.180580A= , LRG_549:g.180580A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264870.8:c.*507A= MANE Select | ENSP00000264870.3:n.*507A= | |
ENST00000264870.7:c.*507A= | ENSP00000264870.3:n.*507A= | |
NM_000129.3:c.*507A= , LRG_549t1:c.*507A= | NP_000120.2:n.*507A= | |
XM_006715010.2:c.*507A= | XP_006715073.1:n.*507A= | |
XM_011514342.1:c.*507A= | XP_011512644.1:n.*507A= | |
NM_000129.4:c.*507A= MANE Select | NP_000120.2:n.*507A= |