HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149570062C>G , CM000664.2:g.149570062C>G | GRCh38 |
NC_000002.11:g.150426576C>G , CM000664.1:g.150426576C>G | GRCh37 |
NC_000002.10:g.150134822C>G | NCBI36 |
NG_009189.1:g.22755G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.803G>C MANE Select | ENSP00000301920.5:p.Ser268Thr | |
ENST00000303319.9:c.803G>C | ENSP00000301920.5:p.Ser268Thr | |
ENST00000422782.2:c.905G>C | ENSP00000408331.2:p.Ser302Thr | |
ENST00000428879.5:c.803G>C | ENSP00000389060.1:p.Ser268Thr | |
NM_015702.2:c.803G>C | NP_056517.1:p.Ser268Thr | |
NM_015702.3:c.803G>C MANE Select | NP_056517.1:p.Ser268Thr |