HGVS | Genome Assembly |
---|---|
NC_000002.12:g.73640952C>G , CM000664.2:g.73640952C>G | GRCh38 |
NC_000002.11:g.73868079C>G , CM000664.1:g.73868079C>G | GRCh37 |
NC_000002.10:g.73721587C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272425.4:c.677G>C MANE Select | ENSP00000272425.3:p.Ser226Thr | |
ENST00000272425.3:c.677G>C | ENSP00000272425.3:p.Ser226Thr | |
NM_003960.3:c.677G>C | NP_003951.3:p.Ser226Thr | |
NM_003960.4:c.677G>C MANE Select | NP_003951.3:p.Ser226Thr |