HGVS | Genome Assembly |
---|---|
NC_000006.12:g.143485160G>C , CM000668.2:g.143485160G>C | GRCh38 |
NC_000006.11:g.143806297G>C , CM000668.1:g.143806297G>C | GRCh37 |
NC_000006.10:g.143847990G>C | NCBI36 |
NG_008459.1:g.39380G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367591.5:c.950G>C MANE Select | ENSP00000356563.4:p.Ser317Thr | |
ENST00000367591.4:c.950G>C | ENSP00000356563.4:p.Ser317Thr | |
ENST00000585848.1:n.89G>C | ||
NM_003630.2:c.950G>C | NP_003621.1:p.Ser317Thr | |
NM_003630.3:c.950G>C MANE Select | NP_003621.1:p.Ser317Thr |