HGVS | Genome Assembly |
---|---|
NC_000006.12:g.6144956C= , CM000668.2:g.6144956C= | GRCh38 |
NC_000006.11:g.6145189C= , CM000668.1:g.6145189C= | GRCh37 |
NC_000006.10:g.6090188C= | NCBI36 |
NG_008107.1:g.180736G= , LRG_549:g.180736G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264870.8:c.*663G= MANE Select | ENSP00000264870.3:n.*663G= | |
ENST00000264870.7:c.*663G= | ENSP00000264870.3:n.*663G= | |
NM_000129.3:c.*663G= , LRG_549t1:c.*663G= | NP_000120.2:n.*663G= | |
XM_006715010.2:c.*663G= | XP_006715073.1:n.*663G= | |
XM_011514342.1:c.*663G= | XP_011512644.1:n.*663G= | |
NM_000129.4:c.*663G= MANE Select | NP_000120.2:n.*663G= |