Linked Data
ClinVar Variation Id:
93768
dbSNP Id:
rs370491691
ExAC:
X:153581299 G / A
gnomAD v2:
X-153581299-G-A
gnomAD v3:
X-154352931-G-A
gnomAD v4:
X-154352931-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154352931G>A , CM000685.2:g.154352931G>A | GRCh38 |
| NC_000023.10:g.153581299G>A , CM000685.1:g.153581299G>A | GRCh37 |
| NC_000023.9:g.153234493G>A | NCBI36 |
| NG_011506.1:g.26708C>T | |
| NG_011506.2:g.26708C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360319.9:c.6203-7C>T | ENSP00000353467.4:n.6203-7C>T | |
| ENST00000369850.10:c.6227-7C>T MANE Select | ENSP00000358866.3:n.6227-7C>T | |
| ENST00000369856.8:c.6146-7C>T | ENSP00000358872.4:n.6146-7C>T | |
| ENST00000422373.6:c.3161-256C>T | ENSP00000416926.2:n.3161-256C>T | |
| ENST00000610817.5:c.6284-7C>T | ENSP00000480593.2:n.6284-7C>T | |
| ENST00000673639.2:c.280-4241C>T | ||
| ENST00000676696.1:c.6506-7C>T | ENSP00000503392.1:n.6506-7C>T | |
| ENST00000678304.1:n.1406-7C>T | ||
| ENST00000344736.8:c.6107-7C>T | ENSP00000358863.3:n.6107-7C>T | |
| ENST00000360319.8:c.6203-7C>T | ENSP00000353467.4:n.6203-7C>T | |
| ENST00000369850.7:c.6227-7C>T | ENSP00000358866.3:n.6227-7C>T | |
| ENST00000369856.7:c.6146-7C>T | ENSP00000358872.4:n.6146-7C>T | |
| ENST00000415241.1:c.429-7C>T | ||
| ENST00000420627.5:c.6183-7C>T | ENSP00000408921.1:n.6183-7C>T | |
| ENST00000422373.5:c.6203-7C>T | ENSP00000416926.1:n.6203-7C>T | |
| ENST00000444578.1:c.170-7C>T | ENSP00000397824.1:n.170-7C>T | |
| ENST00000466325.1:n.435C>T | ||
| ENST00000490936.5:n.2216-7C>T | ||
| ENST00000610817.4:c.5844+462C>T | ENSP00000480593.1:n.5844+462C>T | |
| NM_001110556.1:c.6227-7C>T | NP_001104026.1:n.6227-7C>T | |
| NM_001456.3:c.6203-7C>T | NP_001447.2:n.6203-7C>T | |
| XM_011531127.1:c.6131-7C>T | XP_011529429.1:n.6131-7C>T | |
| XM_011531128.1:c.6107-7C>T | XP_011529430.1:n.6107-7C>T | |
| XM_011531129.1:c.6053-7C>T | XP_011529431.1:n.6053-7C>T | |
| XM_011531130.1:c.6029-7C>T | XP_011529432.1:n.6029-7C>T | |
| XM_011531131.1:c.6026-7C>T | XP_011529433.1:n.6026-7C>T | |
| NM_001110556.2:c.6227-7C>T MANE Select | NP_001104026.1:n.6227-7C>T | |
| NM_001456.4:c.6203-7C>T | NP_001447.2:n.6203-7C>T |