HGVS | Genome Assembly |
---|---|
NC_000018.10:g.13884663C>T , CM000680.2:g.13884663C>T | GRCh38 |
NC_000018.9:g.13884662C>T , CM000680.1:g.13884662C>T | GRCh37 |
NC_000018.8:g.13874662C>T | NCBI36 |
NG_011819.1:g.35874G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000327606.4:c.856G>A MANE Select | ENSP00000333821.2:p.Ala286Thr | |
ENST00000327606.3:c.856G>A | ENSP00000333821.2:p.Ala286Thr | |
NM_000529.2:c.856G>A MANE Select | NP_000520.1:p.Ala286Thr | |
NM_001291911.1:c.856G>A | NP_001278840.1:p.Ala286Thr | |
XM_017025781.1:c.856G>A | XP_016881270.1:p.Ala286Thr |