HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122506782A>C , CM000672.2:g.122506782A>C | GRCh38 |
NC_000010.10:g.124266298A>C , CM000672.1:g.124266298A>C | GRCh37 |
NC_000010.9:g.124256288A>C | NCBI36 |
NG_011554.1:g.50258A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368984.8:c.869A>C MANE Select | ENSP00000357980.3:p.Asn290Thr | |
ENST00000648167.1:c.551A>C | ENSP00000498033.1:p.Asn184Thr | |
ENST00000368984.7:c.869A>C | ENSP00000357980.3:p.Asn290Thr | |
ENST00000420892.1:c.92A>C | ENSP00000412676.1:p.Asn31Thr | |
NM_002775.4:c.869A>C | NP_002766.1:p.Asn290Thr | |
NM_002775.5:c.869A>C MANE Select | NP_002766.1:p.Asn290Thr |