HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52675455C>G , CM000674.2:g.52675455C>G | GRCh38 |
NC_000012.11:g.53069239C>G , CM000674.1:g.53069239C>G | GRCh37 |
NC_000012.10:g.51355506C>G | NCBI36 |
NG_008364.1:g.9953G>C | |
NG_008364.2:g.9953G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252244.3:c.1673G>C MANE Select | ENSP00000252244.3:p.Ser558Thr | |
NM_006121.3:c.1673G>C | NP_006112.3:p.Ser558Thr | |
NM_006121.4:c.1673G>C MANE Select | NP_006112.3:p.Ser558Thr |