HGVS | Genome Assembly |
---|---|
NC_000017.11:g.72123571C>T , CM000679.2:g.72123571C>T | GRCh38 |
NC_000017.10:g.70119712C>T , CM000679.1:g.70119712C>T | GRCh37 |
NC_000017.9:g.67631307C>T | NCBI36 |
NG_012490.1:g.7552C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000245479.3:c.714C>T MANE Select | ENSP00000245479.2:p.Pro238= | |
ENST00000245479.2:c.714C>T | ENSP00000245479.2:p.Pro238= | |
NM_000346.3:c.714C>T | NP_000337.1:p.Pro238= | |
NM_000346.4:c.714C>T MANE Select | NP_000337.1:p.Pro238= |