HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41612519G= , CM000679.2:g.41612519G= | GRCh38 |
NC_000017.10:g.39768771G= , CM000679.1:g.39768771G= | GRCh37 |
NC_000017.9:g.37022297G= | NCBI36 |
NG_008301.1:g.5309C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301653.9:c.170C= MANE Select | ENSP00000301653.3:p.Ser57= | |
ENST00000301653.8:c.170C= | ENSP00000301653.3:p.Ser57= | |
ENST00000588319.1:n.247C= | ||
ENST00000593067.1:c.-312-233C= | ENSP00000467124.1:n.-312-233C= | |
NM_005557.3:c.170C= | NP_005548.2:p.Ser57= | |
NM_005557.4:c.170C= MANE Select | NP_005548.2:p.Ser57= |