HGVS | Genome Assembly |
---|---|
NC_000002.12:g.38071192C>T , CM000664.2:g.38071192C>T | GRCh38 |
NC_000002.11:g.38298335C>T , CM000664.1:g.38298335C>T | GRCh37 |
NC_000002.10:g.38151839C>T | NCBI36 |
NG_008386.2:g.9910G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000490576.2:c.1162G>A | ENSP00000478839.2:p.Ala388Thr | |
ENST00000610745.5:c.1162G>A MANE Select | ENSP00000478561.1:p.Ala388Thr | |
ENST00000492443.1:n.540G>A | ||
ENST00000494864.1:c.49G>A | ENSP00000479876.1:p.Ala17Thr | |
ENST00000610745.4:c.1162G>A | ENSP00000478561.1:p.Ala388Thr | |
ENST00000613082.1:n.557G>A | ||
ENST00000614273.1:c.1162G>A | ENSP00000483678.1:p.Ala388Thr | |
NM_000104.3:c.1162G>A | NP_000095.2:p.Ala388Thr | |
NM_000104.4:c.1162G>A MANE Select | NP_000095.2:p.Ala388Thr |