HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149570051T= , CM000664.2:g.149570051T= | GRCh38 |
NC_000002.11:g.150426565T= , CM000664.1:g.150426565T= | GRCh37 |
NC_000002.10:g.150134811T= | NCBI36 |
NG_009189.1:g.22766A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.814A= MANE Select | ENSP00000301920.5:p.Thr272= | |
ENST00000303319.9:c.814A= | ENSP00000301920.5:p.Thr272= | |
ENST00000422782.2:c.916A= | ENSP00000408331.2:p.Thr306= | |
ENST00000428879.5:c.814A= | ENSP00000389060.1:p.Thr272= | |
NM_015702.2:c.814A= | NP_056517.1:p.Thr272= | |
NM_015702.3:c.814A= MANE Select | NP_056517.1:p.Thr272= |