HGVS | Genome Assembly |
---|---|
NC_000006.12:g.6182121G>A , CM000668.2:g.6182121G>A | GRCh38 |
NC_000006.11:g.6182354G>A , CM000668.1:g.6182354G>A | GRCh37 |
NC_000006.10:g.6127353G>A | NCBI36 |
NG_008107.1:g.143571C>T , LRG_549:g.143571C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264870.8:c.1326C>T MANE Select | ENSP00000264870.3:p.Tyr442= | |
ENST00000264870.7:c.1326C>T | ENSP00000264870.3:p.Tyr442= | |
NM_000129.3:c.1326C>T , LRG_549t1:c.1326C>T | NP_000120.2:p.Tyr442= | |
XM_006715010.2:c.1326C>T | XP_006715073.1:p.Tyr442= | |
XM_011514342.1:c.1488C>T | XP_011512644.1:p.Tyr496= | |
NM_000129.4:c.1326C>T MANE Select | NP_000120.2:p.Tyr442= |