HGVS | Genome Assembly |
---|---|
NC_000023.11:g.50459768G= , CM000685.2:g.50459768G= | GRCh38 |
NC_000023.10:g.50202766G= , CM000685.1:g.50202766G= | GRCh37 |
NC_000023.9:g.50219506G= | NCBI36 |
NG_033143.2:g.15955C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000611977.2:c.645+10266C= MANE Select | ENSP00000477515.1:n.645+10266C= | |
ENST00000611977.1:c.645+10266C= | ENSP00000477515.1:n.645+10266C= | |
NM_001013742.3:c.645+10266C= | NP_001013764.1:n.645+10266C= | |
XM_017029268.2:c.645+10266C= | XP_016884757.1:n.645+10266C= | |
NM_001013742.4:c.645+10266C= MANE Select | NP_001013764.1:n.645+10266C= |