HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148994544A>T , CM000667.2:g.148994544A>T | GRCh38 |
NC_000005.9:g.148374107A>T , CM000667.1:g.148374107A>T | GRCh37 |
NC_000005.8:g.148354300A>T | NCBI36 |
NG_007947.2:g.73631T>A , LRG_269:g.73631T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515425.6:c.*10167T>A MANE Select | ENSP00000423660.1:n.*10167T>A | |
ENST00000504690.5:c.*12+9182T>A | ENSP00000425627.1:n.*12+9182T>A | |
ENST00000510350.1:n.231+12337T>A | ||
NM_024577.3:c.*10167T>A , LRG_269t1:c.*10167T>A | NP_078853.2:n.*10167T>A | |
NM_024577.4:c.*10167T>A MANE Select | NP_078853.2:n.*10167T>A |