HGVS | Genome Assembly |
---|---|
NC_000001.11:g.58576894G= , CM000663.2:g.58576894G= | GRCh38 |
NC_000001.10:g.59042566G= , CM000663.1:g.59042566G= | GRCh37 |
NC_000001.9:g.58815154G= | NCBI36 |
NG_016237.1:g.5601C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371225.4:c.263C= MANE Select | ENSP00000360269.2:p.Thr88= | |
ENST00000371225.3:c.263C= | ENSP00000360269.2:p.Thr88= | |
NM_002353.2:c.263C= | NP_002344.2:p.Thr88= | |
NM_002353.3:c.263C= MANE Select | NP_002344.2:p.Thr88= |