Linked Data
ClinVar Variation Id:
1156869
ClinVar RCV Id:
RCV001499706
dbSNP Id:
rs782396776
ExAC:
X:153609107 C / T
gnomAD v2:
X-153609107-C-T
gnomAD v3:
X-154380747-C-T
gnomAD v4:
X-154380747-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154380747C>T , CM000685.2:g.154380747C>T | GRCh38 |
| NC_000023.10:g.153609107C>T , CM000685.1:g.153609107C>T | GRCh37 |
| NC_000023.9:g.153262301C>T | NCBI36 |
| NG_008677.1:g.11312C>T , LRG_745:g.11312C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682114.1:c.400-6C>T | ENSP00000507245.1:n.400-6C>T | |
| ENST00000682478.1:n.590-6C>T | ||
| ENST00000683576.1:n.590-6C>T | ||
| ENST00000683627.1:c.400-6C>T | ENSP00000507533.1:n.400-6C>T | |
| ENST00000684082.1:c.357-6C>T | ENSP00000508266.1:n.357-6C>T | |
| ENST00000684633.1:n.372-6C>T | ||
| ENST00000684678.1:c.396-6C>T | ENSP00000507059.1:n.396-6C>T | |
| ENST00000369842.9:c.400-6C>T MANE Select | ENSP00000358857.4:n.400-6C>T | |
| ENST00000369835.3:c.295-6C>T | ENSP00000358850.3:n.295-6C>T | |
| ENST00000369842.8:c.400-6C>T | ENSP00000358857.4:n.400-6C>T | |
| ENST00000428228.5:c.*305-6C>T | ENSP00000401081.1:n.*305-6C>T | |
| ENST00000468294.5:n.360-6C>T | ||
| ENST00000471965.1:n.183C>T | ||
| ENST00000485261.1:n.590-6C>T | ||
| ENST00000486738.5:n.758-6C>T | ||
| ENST00000492448.1:n.383-6C>T | ||
| NM_000117.2:c.400-6C>T , LRG_745t1:c.400-6C>T | NP_000108.1:n.400-6C>T | |
| XM_024452349.1:c.406-6C>T | XP_024308117.1:n.406-6C>T | |
| NM_000117.3:c.400-6C>T MANE Select | NP_000108.1:n.400-6C>T |