HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6710838T>G , CM000681.2:g.6710838T>G | GRCh38 |
NC_000019.9:g.6710849T>G , CM000681.1:g.6710849T>G | GRCh37 |
NC_000019.8:g.6661849T>G | NCBI36 |
NG_009557.1:g.14814A>C , LRG_27:g.14814A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000695652.1:c.1364A>C | ENSP00000512083.1:p.Asn455Thr | |
ENST00000695654.1:c.611A>C | ENSP00000512085.1:p.Asn204Thr | |
ENST00000695655.1:c.392A>C | ENSP00000512086.1:p.Asn131Thr | |
ENST00000695692.1:n.851A>C | ||
ENST00000245907.11:c.1487A>C MANE Select | ENSP00000245907.4:p.Asn496Thr | |
ENST00000245907.10:c.1487A>C | ENSP00000245907.4:p.Asn496Thr | |
ENST00000600763.1:n.120A>C | ||
NM_000064.3:c.1487A>C | NP_000055.2:p.Asn496Thr | |
NM_000064.4:c.1487A>C MANE Select | NP_000055.2:p.Asn496Thr |