HGVS | Genome Assembly |
---|---|
NC_000009.12:g.6595031G= , CM000671.2:g.6595031G= | GRCh38 |
NC_000009.11:g.6595031G= , CM000671.1:g.6595031G= | GRCh37 |
NC_000009.10:g.6585031G= | NCBI36 |
NG_016397.1:g.55662C= , LRG_643:g.55662C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321612.8:c.1244C= MANE Select | ENSP00000370737.4:p.Thr415= | |
ENST00000638654.1:c.491C= | ENSP00000491101.1:p.Thr164= | |
ENST00000639364.1:n.944C= | ||
ENST00000639443.1:n.812C= | ||
ENST00000639493.1:n.396C= | ||
ENST00000639954.1:n.952C= | ||
ENST00000640592.1:n.1127C= | ||
ENST00000321612.6:c.1244C= | ENSP00000370737.3:p.Thr415= | |
ENST00000463305.1:n.328C= | ||
NM_000170.2:c.1244C= , LRG_643t1:c.1244C= | NP_000161.2:p.Thr415= | |
NM_000170.3:c.1244C= MANE Select | NP_000161.2:p.Thr415= |