HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148994573T>C , CM000667.2:g.148994573T>C | GRCh38 |
NC_000005.9:g.148374136T>C , CM000667.1:g.148374136T>C | GRCh37 |
NC_000005.8:g.148354329T>C | NCBI36 |
NG_007947.2:g.73602A>G , LRG_269:g.73602A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515425.6:c.*10138A>G MANE Select | ENSP00000423660.1:n.*10138A>G | |
ENST00000504690.5:c.*12+9153A>G | ENSP00000425627.1:n.*12+9153A>G | |
ENST00000510350.1:n.231+12308A>G | ||
NM_024577.3:c.*10138A>G , LRG_269t1:c.*10138A>G | NP_078853.2:n.*10138A>G | |
NM_024577.4:c.*10138A>G MANE Select | NP_078853.2:n.*10138A>G |