HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67583832G>T , CM000673.2:g.67583832G>T | GRCh38 |
NC_000011.9:g.67351303G>T , CM000673.1:g.67351303G>T | GRCh37 |
NC_000011.8:g.67107879G>T | NCBI36 |
NG_012075.1:g.5238G>T , LRG_723:g.5238G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000398603.6:c.-12G>T | ENSP00000381604.1:n.-12G>T | |
ENST00000398606.10:c.-12G>T MANE Select | ENSP00000381607.3:n.-12G>T | |
ENST00000646888.1:c.-12G>T | ENSP00000494477.1:n.-12G>T | |
ENST00000398603.5:c.-12G>T | ENSP00000381604.1:n.-12G>T | |
ENST00000398606.7:c.-12G>T | ENSP00000381607.3:n.-12G>T | |
ENST00000494593.1:n.11G>T | ||
NM_000852.3:c.-12G>T , LRG_723t1:c.-12G>T | NP_000843.1:n.-12G>T | |
NM_000852.4:c.-12G>T MANE Select | NP_000843.1:n.-12G>T |