HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4912494T= , CM000674.2:g.4912494T= | GRCh38 |
NC_000012.11:g.5021660T= , CM000674.1:g.5021660T= | GRCh37 |
NC_000012.10:g.4891921T= | NCBI36 |
NG_011815.1:g.7588T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382545.5:c.1116T= MANE Select | ENSP00000371985.3:p.Thr372= | |
ENST00000543874.3:n.105+2022T= | ||
ENST00000639306.1:c.954T= | ENSP00000492506.1:p.Thr318= | |
ENST00000639680.1:c.76+228T= | ||
ENST00000382545.3:c.1116T= | ENSP00000371985.3:p.Thr372= | |
ENST00000541095.1:n.105+2022T= | ||
ENST00000543874.2:n.96+2022T= | ||
NM_000217.2:c.1116T= | NP_000208.2:p.Thr372= | |
NM_000217.3:c.1116T= MANE Select | NP_000208.2:p.Thr372= |