HGVS | Genome Assembly |
---|---|
NC_000010.11:g.129767006A>C , CM000672.2:g.129767006A>C | GRCh38 |
NC_000010.10:g.131565270A>C , CM000672.1:g.131565270A>C | GRCh37 |
NC_000010.9:g.131455260A>C | NCBI36 |
NG_052673.1:g.304823A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000306010.8:c.*9A>C | ENSP00000302111.7:n.*9A>C | |
ENST00000651593.1:c.*9A>C MANE Select | ENSP00000498729.1:n.*9A>C | |
ENST00000306010.7:c.*9A>C | ENSP00000302111.7:n.*9A>C | |
NM_002412.3:c.*9A>C | NP_002403.2:n.*9A>C | |
NM_002412.4:c.*9A>C | NP_002403.2:n.*9A>C | |
XM_005252682.2:c.*9A>C | XP_005252739.1:n.*9A>C | |
XM_006717863.2:c.*9A>C | XP_006717926.1:n.*9A>C | |
XM_011539817.1:c.*9A>C | XP_011538119.1:n.*9A>C | |
NM_002412.5:c.*9A>C MANE Select | NP_002403.3:n.*9A>C | |
XM_017016275.1:c.*9A>C | XP_016871764.1:n.*9A>C |