HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190563T>A , CM000663.2:g.204190563T>A | GRCh38 |
NC_000001.10:g.204159691T>A , CM000663.1:g.204159691T>A | GRCh37 |
NC_000001.9:g.202426314T>A | NCBI36 |
NG_032151.1:g.10929A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.338A>T MANE Select | ENSP00000356162.4:p.Asn113Ile | |
ENST00000367194.4:c.338A>T | ENSP00000356162.4:p.Asn113Ile | |
ENST00000625357.1:c.338A>T | ENSP00000485957.1:p.Asn113Ile | |
NM_002256.3:c.338A>T | NP_002247.3:p.Asn113Ile | |
XM_011509525.1:c.338A>T | XP_011507827.1:p.Asn113Ile | |
NM_002256.4:c.338A>T MANE Select | NP_002247.3:p.Asn113Ile |