HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215640732G>T , CM000663.2:g.215640732G>T | GRCh38 |
NC_000001.10:g.215814074G>T , CM000663.1:g.215814074G>T | GRCh37 |
NC_000001.9:g.213880697G>T | NCBI36 |
NG_009497.1:g.787665C>A | |
NG_009497.2:g.787717C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.14794C>A MANE Select | ENSP00000305941.3:p.Pro4932Thr | |
ENST00000674083.1:c.14794C>A | ENSP00000501296.1:p.Pro4932Thr | |
ENST00000307340.7:c.14794C>A | ENSP00000305941.3:p.Pro4932Thr | |
NM_206933.2:c.14794C>A | NP_996816.2:p.Pro4932Thr | |
NM_206933.3:c.14794C>A | NP_996816.2:p.Pro4932Thr | |
NM_206933.4:c.14794C>A MANE Select | NP_996816.3:p.Pro4932Thr |