Linked Data
gnomAD v4:
X-154379421-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154379421G>A , CM000685.2:g.154379421G>A | GRCh38 |
| NC_000023.10:g.153607781G>A , CM000685.1:g.153607781G>A | GRCh37 |
| NC_000023.9:g.153260975G>A | NCBI36 |
| NG_008677.1:g.9986G>A , LRG_745:g.9986G>A | |
| NG_011506.1:g.226C>T | |
| NG_011506.2:g.218C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682114.1:c.-64G>A | ENSP00000507245.1:n.-64G>A | |
| ENST00000369842.9:c.-64G>A MANE Select | ENSP00000358857.4:n.-64G>A | |
| ENST00000369835.3:c.-64G>A | ENSP00000358850.3:n.-64G>A | |
| ENST00000369842.8:c.-64G>A | ENSP00000358857.4:n.-64G>A | |
| ENST00000428228.5:c.-64G>A | ENSP00000401081.1:n.-64G>A | |
| ENST00000485261.1:n.18G>A | ||
| ENST00000486738.5:n.81G>A | ||
| NM_000117.2:c.-64G>A , LRG_745t1:c.-64G>A | NP_000108.1:n.-64G>A | |
| XM_024452349.1:c.-272G>A | XP_024308117.1:n.-272G>A | |
| NM_000117.3:c.-64G>A MANE Select | NP_000108.1:n.-64G>A |