HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32813337G>T , CM000668.2:g.32813337G>T | GRCh38 |
NC_000006.11:g.32781114G>T , CM000668.1:g.32781114G>T | GRCh37 |
NC_000006.10:g.32889092G>T | NCBI36 |
NG_009793.3:g.30434C>A | |
NG_012008.1:g.8712C>A | |
NG_009793.4:g.30434C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000438763.7:c.787-86C>A MANE Select | ENSP00000390020.2:n.787-86C>A | |
ENST00000648009.1:c.787-86C>A | ENSP00000496848.1:n.787-86C>A | |
ENST00000438763.6:c.787-86C>A | ENSP00000390020.2:n.787-86C>A | |
ENST00000475235.1:n.1310-86C>A | ||
ENST00000488325.5:c.*558-86C>A | ENSP00000436618.1:n.*558-86C>A | |
NM_002120.3:c.787-86C>A | NP_002111.1:n.787-86C>A | |
NM_002120.4:c.787-86C>A MANE Select | NP_002111.1:n.787-86C>A |