HGVS | Genome Assembly |
---|---|
NC_000016.10:g.30737277C>T , CM000678.2:g.30737277C>T | GRCh38 |
NC_000016.9:g.30748598C>T , CM000678.1:g.30748598C>T | GRCh37 |
NC_000016.8:g.30656099C>T | NCBI36 |
NG_032135.1:g.43137C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000411466.7:c.7237C>T | ENSP00000405186.3:p.Pro2413Ser | |
ENST00000704023.1:c.1517C>T | ||
ENST00000706321.1:c.7237C>T | ENSP00000516346.1:p.Pro2413Ser | |
ENST00000262518.9:c.7237C>T MANE Select | ENSP00000262518.4:p.Pro2413Ser | |
ENST00000262518.8:c.7237C>T | ENSP00000262518.4:p.Pro2413Ser | |
ENST00000380361.7:c.6706C>T | ENSP00000369719.3:p.Pro2236Ser | |
ENST00000395059.6:c.6460C>T | ENSP00000378499.3:p.Pro2154Ser | |
NM_006662.2:c.7237C>T | NP_006653.2:p.Pro2413Ser | |
NM_006662.3:c.7237C>T MANE Select | NP_006653.2:p.Pro2413Ser |