HGVS | Genome Assembly |
---|---|
NC_000006.12:g.6181960_6181963del , CM000668.2:g.6181960_6181963del | GRCh38 |
NC_000006.11:g.6182193_6182196del , CM000668.1:g.6182193_6182196del | GRCh37 |
NC_000006.10:g.6127192_6127195del | NCBI36 |
NG_008107.1:g.143733_143736del , LRG_549:g.143733_143736del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264870.8:c.1459+29_1459+32del MANE Select | ENSP00000264870.3:n.1459+29_1459+32del | |
ENST00000264870.7:c.1459+29_1459+32del | ENSP00000264870.3:n.1459+29_1459+32del | |
NM_000129.3:c.1459+29_1459+32del , LRG_549t1:c.1459+29_1459+32del | NP_000120.2:n.1459+29_1459+32del | |
XM_006715010.2:c.1459+29_1459+32del | XP_006715073.1:n.1459+29_1459+32del | |
XM_011514342.1:c.1621+29_1621+32del | XP_011512644.1:n.1621+29_1621+32del | |
NM_000129.4:c.1459+29_1459+32del MANE Select | NP_000120.2:n.1459+29_1459+32del |