HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663089T>A , CM000676.2:g.36663089T>A | GRCh38 |
NC_000014.8:g.37132294T>A , CM000676.1:g.37132294T>A | GRCh37 |
NC_000014.7:g.36202045T>A | NCBI36 |
NG_013357.1:g.10522T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361487.7:c.197T>A MANE Select | ENSP00000355245.6:p.Ile66Asn | |
ENST00000555639.2:c.197T>A | ENSP00000501203.1:p.Ile66Asn | |
ENST00000361487.6:c.197T>A | ENSP00000355245.6:p.Ile66Asn | |
ENST00000402703.6:c.197T>A | ENSP00000384817.2:p.Ile66Asn | |
ENST00000554201.1:c.-365T>A | ENSP00000450434.1:n.-365T>A | |
ENST00000555639.1:n.499T>A | ||
NM_006194.3:c.197T>A | NP_006185.1:p.Ile66Asn | |
NM_001372076.1:c.197T>A MANE Select | NP_001359005.1:p.Ile66Asn | |
NM_006194.4:c.197T>A | NP_006185.1:p.Ile66Asn |