HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67583836T>A , CM000673.2:g.67583836T>A | GRCh38 |
NC_000011.9:g.67351307T>A , CM000673.1:g.67351307T>A | GRCh37 |
NC_000011.8:g.67107883T>A | NCBI36 |
NG_012075.1:g.5242T>A , LRG_723:g.5242T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000398603.6:c.-8T>A | ENSP00000381604.1:n.-8T>A | |
ENST00000398606.10:c.-8T>A MANE Select | ENSP00000381607.3:n.-8T>A | |
ENST00000646888.1:c.-8T>A | ENSP00000494477.1:n.-8T>A | |
ENST00000398603.5:c.-8T>A | ENSP00000381604.1:n.-8T>A | |
ENST00000398606.7:c.-8T>A | ENSP00000381607.3:n.-8T>A | |
ENST00000494593.1:n.15T>A | ||
NM_000852.3:c.-8T>A , LRG_723t1:c.-8T>A | NP_000843.1:n.-8T>A | |
NM_000852.4:c.-8T>A MANE Select | NP_000843.1:n.-8T>A |