HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133352662T= , CM000671.2:g.133352662T= | GRCh38 |
NC_000009.10:g.135209338T= | NCBI36 |
NG_008477.1:g.8845A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371974.8:c.588+32A= MANE Select | ENSP00000361042.3:n.588+32A= | |
ENST00000371974.7:c.588+32A= | ENSP00000361042.3:n.588+32A= | |
ENST00000437995.1:n.498+32A= | ||
ENST00000495952.5:n.578+32A= | ||
ENST00000615505.4:c.261+32A= | ENSP00000482067.1:n.261+32A= | |
NM_001280787.1:c.261+32A= | NP_001267716.1:n.261+32A= | |
NM_003172.3:c.588+32A= | NP_003163.1:n.588+32A= | |
XM_011518942.1:c.261+32A= | XP_011517244.1:n.261+32A= | |
NM_003172.4:c.588+32A= MANE Select | NP_003163.1:n.588+32A= |