HGVS | Genome Assembly |
---|---|
NC_000017.11:g.82727247T>A , CM000679.2:g.82727247T>A | GRCh38 |
NC_000017.10:g.80685123T>A , CM000679.1:g.80685123T>A | GRCh37 |
NC_000017.9:g.78278412T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269373.11:c.*76T>A MANE Select | ENSP00000269373.6:n.*76T>A | |
ENST00000269373.10:c.*76T>A | ENSP00000269373.6:n.*76T>A | |
ENST00000571594.1:c.53+80T>A | ENSP00000459751.1:n.53+80T>A | |
ENST00000574832.5:c.*963T>A | ENSP00000460869.1:n.*963T>A | |
NM_024619.3:c.*76T>A | NP_078895.2:n.*76T>A | |
NR_046408.1:n.1184T>A | ||
XM_024450948.1:c.*76T>A | XP_024306716.1:n.*76T>A | |
NM_024619.4:c.*76T>A MANE Select | NP_078895.2:n.*76T>A | |
NR_046408.2:n.1184T>A |