HGVS | Genome Assembly |
---|---|
NC_000023.11:g.121048450A>T , CM000685.2:g.121048450A>T | GRCh38 |
NC_000023.10:g.120182304A>T , CM000685.1:g.120182304A>T | GRCh37 |
NC_000023.9:g.120009985A>T | NCBI36 |
NG_016456.1:g.5843A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000328078.3:c.766A>T MANE Select | ENSP00000327589.1:p.Thr256Ser | |
ENST00000328078.2:c.766A>T | ENSP00000327589.1:p.Thr256Ser | |
NM_012084.3:c.766A>T | NP_036216.2:p.Thr256Ser | |
NM_012084.4:c.766A>T MANE Select | NP_036216.2:p.Thr256Ser |