HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55151796A>G , CM000681.2:g.55151796A>G | GRCh38 |
NC_000019.9:g.55663164A>G , CM000681.1:g.55663164A>G | GRCh37 |
NC_000019.8:g.60354976A>G | NCBI36 |
NG_007866.2:g.10937T>C , LRG_432:g.10937T>C | |
NG_011829.2:g.2443T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.*38T>C MANE Select | ENSP00000341838.5:n.*38T>C | |
ENST00000665070.1:c.*38T>C | ENSP00000499482.1:n.*38T>C | |
ENST00000344887.9:c.*38T>C | ENSP00000341838.5:n.*38T>C | |
ENST00000585806.5:n.670T>C | ||
ENST00000588882.1:c.*38T>C | ENSP00000466729.1:n.*38T>C | |
ENST00000589864.1:n.499T>C | ||
NM_000363.4:c.*38T>C , LRG_432t1:c.*38T>C | NP_000354.4:n.*38T>C | |
NM_000363.5:c.*38T>C MANE Select | NP_000354.4:n.*38T>C |