HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225312G= , CM000668.2:g.3225312G= | GRCh38 |
NC_000006.11:g.3225546G= , CM000668.1:g.3225546G= | GRCh37 |
NC_000006.10:g.3170545G= | NCBI36 |
NG_016715.1:g.7423C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000259818.8:c.777C= MANE Select | ENSP00000259818.6:p.Pro259= | |
ENST00000680070.1:n.1707C= | ||
ENST00000681707.1:n.1604C= | ||
ENST00000681757.1:n.1082C= | ||
ENST00000259818.7:c.777C= | ENSP00000259818.6:p.Pro259= | |
ENST00000473006.1:n.894C= | ||
NM_178012.4:c.777C= | NP_821080.1:p.Pro259= | |
XM_011514571.1:c.561C= | XP_011512873.1:p.Pro187= | |
NM_178012.5:c.777C= MANE Select | NP_821080.1:p.Pro259= |