HGVS | Genome Assembly |
---|---|
NC_000002.12:g.38071181G>A , CM000664.2:g.38071181G>A | GRCh38 |
NC_000002.11:g.38298324G>A , CM000664.1:g.38298324G>A | GRCh37 |
NC_000002.10:g.38151828G>A | NCBI36 |
NG_008386.2:g.9921C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000490576.2:c.1173C>T | ENSP00000478839.2:p.Phe391= | |
ENST00000610745.5:c.1173C>T MANE Select | ENSP00000478561.1:p.Phe391= | |
ENST00000492443.1:n.551C>T | ||
ENST00000494864.1:c.60C>T | ENSP00000479876.1:p.Phe20= | |
ENST00000610745.4:c.1173C>T | ENSP00000478561.1:p.Phe391= | |
ENST00000613082.1:n.568C>T | ||
ENST00000614273.1:c.1173C>T | ENSP00000483678.1:p.Phe391= | |
NM_000104.3:c.1173C>T | NP_000095.2:p.Phe391= | |
NM_000104.4:c.1173C>T MANE Select | NP_000095.2:p.Phe391= |