HGVS | Genome Assembly |
---|---|
NC_000016.10:g.177215G>A , CM000678.2:g.177215G>A | GRCh38 |
NC_000016.9:g.227214G>A , CM000678.1:g.227214G>A | GRCh37 |
NC_000016.8:g.167214G>A | NCBI36 |
NG_000006.1:g.38078G>A | |
NG_059186.1:g.5565G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320868.9:c.301-68G>A MANE Select | ENSP00000322421.5:n.301-68G>A | |
ENST00000397797.1:c.205-68G>A | ENSP00000380899.1:n.205-68G>A | |
ENST00000472694.1:n.437-68G>A | ||
ENST00000487791.1:n.351G>A | ||
NM_000558.4:c.301-68G>A | NP_000549.1:n.301-68G>A | |
NM_000558.5:c.301-68G>A MANE Select | NP_000549.1:n.301-68G>A |