HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128848001T>C , CM000669.2:g.128848001T>C | GRCh38 |
NC_000007.13:g.128488055T>C , CM000669.1:g.128488055T>C | GRCh37 |
NC_000007.12:g.128275291T>C | NCBI36 |
NG_011807.1:g.22573T>C , LRG_870:g.22573T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.4513T>C MANE Select | ENSP00000327145.8:p.Tyr1505His | |
ENST00000325888.12:c.4513T>C | ENSP00000327145.8:p.Tyr1505His | |
ENST00000346177.6:c.4513T>C | ENSP00000344002.6:p.Tyr1505His | |
NM_001127487.1:c.4513T>C | NP_001120959.1:p.Tyr1505His | |
NM_001458.4:c.4513T>C , LRG_870t1:c.4513T>C | NP_001449.3:p.Tyr1505His | |
NM_001127487.2:c.4513T>C | NP_001120959.1:p.Tyr1505His | |
NM_001458.5:c.4513T>C MANE Select | NP_001449.3:p.Tyr1505His |