HGVS | Genome Assembly |
---|---|
NC_000019.10:g.4816639T>G , CM000681.2:g.4816639T>G | GRCh38 |
NC_000019.9:g.4816651T>G , CM000681.1:g.4816651T>G | GRCh37 |
NC_000019.8:g.4767651T>G | NCBI36 |
NG_031998.1:g.20104A>C , LRG_358:g.20104A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248244.6:c.1739A>C MANE Select | ENSP00000248244.4:p.Tyr580Ser | |
ENST00000248244.5:c.1739A>C | ENSP00000248244.4:p.Tyr580Ser | |
ENST00000621756.1:c.1322A>C | ENSP00000479467.1:p.Tyr441Ser | |
NM_182919.3:c.1739A>C , LRG_358t1:c.1739A>C | NP_891549.1:p.Tyr580Ser | |
NM_001385678.1:c.1697A>C | NP_001372607.1:p.Tyr566Ser | |
NM_001385679.1:c.1604A>C | NP_001372608.1:p.Tyr535Ser | |
NM_001385680.1:c.1097A>C | NP_001372609.1:p.Tyr366Ser | |
NM_182919.4:c.1739A>C MANE Select | NP_891549.1:p.Tyr580Ser |