HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67583828C= , CM000673.2:g.67583828C= | GRCh38 |
NC_000011.9:g.67351299C= , CM000673.1:g.67351299C= | GRCh37 |
NC_000011.8:g.67107875C= | NCBI36 |
NG_012075.1:g.5234C= , LRG_723:g.5234C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000398603.6:c.-16C= | ENSP00000381604.1:n.-16C= | |
ENST00000398606.10:c.-16C= MANE Select | ENSP00000381607.3:n.-16C= | |
ENST00000646888.1:c.-16C= | ENSP00000494477.1:n.-16C= | |
ENST00000398603.5:c.-16C= | ENSP00000381604.1:n.-16C= | |
ENST00000398606.7:c.-16C= | ENSP00000381607.3:n.-16C= | |
ENST00000494593.1:n.7C= | ||
NM_000852.3:c.-16C= , LRG_723t1:c.-16C= | NP_000843.1:n.-16C= | |
NM_000852.4:c.-16C= MANE Select | NP_000843.1:n.-16C= |