HGVS | Genome Assembly |
---|---|
NC_000012.12:g.69353606A>C , CM000674.2:g.69353606A>C | GRCh38 |
NC_000012.11:g.69747386A>C , CM000674.1:g.69747386A>C | GRCh37 |
NC_000012.10:g.68033653A>C | NCBI36 |
NG_008195.1:g.10253A>C , LRG_768:g.10253A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261267.7:c.*387A>C MANE Select | ENSP00000261267.2:n.*387A>C | |
ENST00000261267.6:c.*387A>C | ENSP00000261267.2:n.*387A>C | |
NM_000239.2:c.*387A>C , LRG_768t1:c.*387A>C | NP_000230.1:n.*387A>C | |
NM_000239.3:c.*387A>C MANE Select | NP_000230.1:n.*387A>C |