HGVS | Genome Assembly |
---|---|
NC_000009.12:g.98542031C>T , CM000671.2:g.98542031C>T | GRCh38 |
NC_000009.11:g.101304313C>T , CM000671.1:g.101304313C>T | GRCh37 |
NC_000009.10:g.100344134C>T | NCBI36 |
NG_016426.1:g.172167G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259455.4:c.472G>A MANE Select | ENSP00000259455.2:p.Ala158Thr | |
ENST00000637410.1:n.250G>A | ||
ENST00000637717.1:c.88G>A | ENSP00000490789.1:p.Ala30Thr | |
ENST00000638001.1:n.82G>A | ||
ENST00000259455.3:c.472G>A | ENSP00000259455.2:p.Ala158Thr | |
ENST00000477471.1:n.259G>A | ||
ENST00000634227.1:n.246G>A | ||
NM_005458.7:c.472G>A | NP_005449.5:p.Ala158Thr | |
XM_017015331.2:c.178G>A | XP_016870820.1:p.Ala60Thr | |
NM_005458.8:c.472G>A MANE Select | NP_005449.5:p.Ala158Thr |