HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73323441G>A , CM000677.2:g.73323441G>A | GRCh38 |
NC_000015.9:g.73615782G>A , CM000677.1:g.73615782G>A | GRCh37 |
NC_000015.8:g.71402835G>A | NCBI36 |
NG_009063.1:g.50824C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261917.4:c.2652C>T MANE Select | ENSP00000261917.3:p.Pro884= | |
ENST00000261917.3:c.2652C>T | ENSP00000261917.3:p.Pro884= | |
NM_005477.2:c.2652C>T | NP_005468.1:p.Pro884= | |
XM_011521148.1:c.1434C>T | XP_011519450.1:p.Pro478= | |
XM_011521148.2:c.1434C>T | XP_011519450.1:p.Pro478= | |
NM_005477.3:c.2652C>T MANE Select | NP_005468.1:p.Pro884= |