HGVS | Genome Assembly |
---|---|
NC_000009.12:g.98541980T>C , CM000671.2:g.98541980T>C | GRCh38 |
NC_000009.11:g.101304262T>C , CM000671.1:g.101304262T>C | GRCh37 |
NC_000009.10:g.100344083T>C | NCBI36 |
NG_016426.1:g.172218A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000259455.4:c.523A>G MANE Select | ENSP00000259455.2:p.Thr175Ala | |
ENST00000637410.1:n.301A>G | ||
ENST00000637717.1:c.139A>G | ENSP00000490789.1:p.Thr47Ala | |
ENST00000259455.3:c.523A>G | ENSP00000259455.2:p.Thr175Ala | |
ENST00000477471.1:n.310A>G | ||
ENST00000634227.1:n.297A>G | ||
NM_005458.7:c.523A>G | NP_005449.5:p.Thr175Ala | |
XM_017015331.2:c.229A>G | XP_016870820.1:p.Thr77Ala | |
NM_005458.8:c.523A>G MANE Select | NP_005449.5:p.Thr175Ala |