HGVS | Genome Assembly |
---|---|
NC_000016.10:g.81357911A>T , CM000678.2:g.81357911A>T | GRCh38 |
NC_000016.9:g.81391516A>T , CM000678.1:g.81391516A>T | GRCh37 |
NC_000016.8:g.79949017A>T | NCBI36 |
NG_009007.1:g.47946A>T , LRG_242:g.47946A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648349.2:c.*661A>T | ENSP00000498114.1:n.*661A>T | |
ENST00000648994.2:c.953A>T MANE Select | ENSP00000497351.1:p.Asn318Ile | |
ENST00000650388.1:c.487A>T | ENSP00000498081.1:n.487A>T | |
ENST00000568107.2:c.953A>T | ENSP00000476795.1:p.Asn318Ile | |
NM_022041.3:c.953A>T , LRG_242t1:c.953A>T | NP_071324.1:p.Asn318Ile | |
XM_017023734.1:c.314A>T | XP_016879223.1:p.Asn105Ile | |
NM_001377486.1:c.314A>T | NP_001364415.1:p.Asn105Ile | |
NM_022041.4:c.953A>T MANE Select | NP_071324.1:p.Asn318Ile |