HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67583835T>C , CM000673.2:g.67583835T>C | GRCh38 |
NC_000011.9:g.67351306T>C , CM000673.1:g.67351306T>C | GRCh37 |
NC_000011.8:g.67107882T>C | NCBI36 |
NG_012075.1:g.5241T>C , LRG_723:g.5241T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000398603.6:c.-9T>C | ENSP00000381604.1:n.-9T>C | |
ENST00000398606.10:c.-9T>C MANE Select | ENSP00000381607.3:n.-9T>C | |
ENST00000646888.1:c.-9T>C | ENSP00000494477.1:n.-9T>C | |
ENST00000398603.5:c.-9T>C | ENSP00000381604.1:n.-9T>C | |
ENST00000398606.7:c.-9T>C | ENSP00000381607.3:n.-9T>C | |
ENST00000494593.1:n.14T>C | ||
NM_000852.3:c.-9T>C , LRG_723t1:c.-9T>C | NP_000843.1:n.-9T>C | |
NM_000852.4:c.-9T>C MANE Select | NP_000843.1:n.-9T>C |