HGVS | Genome Assembly |
---|---|
NC_000009.12:g.98542026G>T , CM000671.2:g.98542026G>T | GRCh38 |
NC_000009.11:g.101304308G>T , CM000671.1:g.101304308G>T | GRCh37 |
NC_000009.10:g.100344129G>T | NCBI36 |
NG_016426.1:g.172172C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259455.4:c.477C>A MANE Select | ENSP00000259455.2:p.Thr159= | |
ENST00000637410.1:n.255C>A | ||
ENST00000637717.1:c.93C>A | ENSP00000490789.1:p.Thr31= | |
ENST00000638001.1:n.87C>A | ||
ENST00000259455.3:c.477C>A | ENSP00000259455.2:p.Thr159= | |
ENST00000477471.1:n.264C>A | ||
ENST00000634227.1:n.251C>A | ||
NM_005458.7:c.477C>A | NP_005449.5:p.Thr159= | |
XM_017015331.2:c.183C>A | XP_016870820.1:p.Thr61= | |
NM_005458.8:c.477C>A MANE Select | NP_005449.5:p.Thr159= |