HGVS | Genome Assembly |
---|---|
NC_000023.11:g.38411907C>T , CM000685.2:g.38411907C>T | GRCh38 |
NC_000023.10:g.38271160C>T , CM000685.1:g.38271160C>T | GRCh37 |
NC_000023.9:g.38156104C>T | NCBI36 |
NG_008471.1:g.64425C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000039007.5:c.913C>T MANE Select | ENSP00000039007.4:p.Pro305Ser | |
ENST00000643344.1:c.*663C>T | ENSP00000496606.1:n.*663C>T | |
ENST00000039007.4:c.913C>T | ENSP00000039007.4:p.Pro305Ser | |
ENST00000465127.1:c.172-254214C>T | ENSP00000417050.1:n.172-254214C>T | |
NM_000531.5:c.913C>T | NP_000522.3:p.Pro305Ser | |
NM_000531.6:c.913C>T MANE Select | NP_000522.3:p.Pro305Ser |