HGVS | Genome Assembly |
---|---|
NC_000023.11:g.9741329T>A , CM000685.2:g.9741329T>A | GRCh38 |
NC_000023.10:g.9709369T>A , CM000685.1:g.9709369T>A | GRCh37 |
NC_000023.9:g.9669369T>A | NCBI36 |
NG_009074.1:g.29549A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000467482.6:c.885+9A>T MANE Select | ENSP00000417161.1:n.885+9A>T | |
ENST00000447366.5:c.633+9A>T | ENSP00000390546.2:n.633+9A>T | |
ENST00000467482.5:c.885+9A>T | ENSP00000417161.1:n.885+9A>T | |
NM_000273.2:c.885+9A>T | NP_000264.2:n.885+9A>T | |
XM_005274541.2:c.885+9A>T | XP_005274598.1:n.885+9A>T | |
XM_005274541.3:c.885+9A>T | XP_005274598.1:n.885+9A>T | |
XM_024452387.1:c.633+9A>T | XP_024308155.1:n.633+9A>T | |
XM_024452388.1:c.633+9A>T | XP_024308156.1:n.633+9A>T | |
NM_000273.3:c.885+9A>T MANE Select | NP_000264.2:n.885+9A>T |