HGVS | Genome Assembly |
---|---|
NC_000009.12:g.98541607T>C , CM000671.2:g.98541607T>C | GRCh38 |
NC_000009.11:g.101303889T>C , CM000671.1:g.101303889T>C | GRCh37 |
NC_000009.10:g.100343710T>C | NCBI36 |
NG_016426.1:g.172591A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259455.4:c.630+266A>G MANE Select | ENSP00000259455.2:n.630+266A>G | |
ENST00000637410.1:n.408+266A>G | ||
ENST00000259455.3:c.630+266A>G | ENSP00000259455.2:n.630+266A>G | |
ENST00000477471.1:n.417+266A>G | ||
ENST00000634227.1:n.404+266A>G | ||
NM_005458.7:c.630+266A>G | NP_005449.5:n.630+266A>G | |
XM_017015331.2:c.336+266A>G | XP_016870820.1:n.336+266A>G | |
NM_005458.8:c.630+266A>G MANE Select | NP_005449.5:n.630+266A>G |