HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57763706G>C , CM000674.2:g.57763706G>C | GRCh38 |
NC_000012.11:g.58157489G>C , CM000674.1:g.58157489G>C | GRCh37 |
NC_000012.10:g.56443756G>C | NCBI36 |
NG_007076.1:g.8488C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000713544.1:c.1399C>G | ENSP00000518840.1:p.Pro467Ala | |
ENST00000713545.1:c.*323C>G | ENSP00000518841.1:n.*323C>G | |
ENST00000228606.9:c.1318C>G MANE Select | ENSP00000228606.4:p.Pro440Ala | |
ENST00000228606.8:c.1318C>G | ENSP00000228606.4:p.Pro440Ala | |
ENST00000547344.5:n.1457C>G | ||
NM_000785.3:c.1318C>G | NP_000776.1:p.Pro440Ala | |
NM_000785.4:c.1318C>G MANE Select | NP_000776.1:p.Pro440Ala |