Linked Data
ClinVar Variation Id:
166820
dbSNP Id:
rs727503846
ExAC:
X:18631384 A / T
gnomAD v2:
X-18631384-A-T
gnomAD v4:
X-18613264-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.18613264A>T , CM000685.2:g.18613264A>T | GRCh38 |
| NC_000023.10:g.18631384A>T , CM000685.1:g.18631384A>T | GRCh37 |
| NC_000023.9:g.18541305A>T | NCBI36 |
| NG_008475.1:g.192660A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000623535.2:c.2265A>T MANE Select | ENSP00000485244.1:p.Ala755= | |
| ENST00000635828.1:c.2265A>T | ENSP00000490170.1:p.Ala755= | |
| ENST00000674046.1:c.2265A>T | ENSP00000501174.1:p.Ala755= | |
| ENST00000379989.6:c.2265A>T | ENSP00000369325.3:p.Ala755= | |
| ENST00000379996.7:c.2265A>T | ENSP00000369332.3:p.Ala755= | |
| ENST00000463994.4:c.2265A>T | ENSP00000485184.1:p.Ala755= | |
| ENST00000623535.1:c.2265A>T | ENSP00000485244.1:p.Ala755= | |
| NM_001037343.1:c.2265A>T | NP_001032420.1:p.Ala755= | |
| NM_003159.2:c.2265A>T | NP_003150.1:p.Ala755= | |
| XM_011545569.1:c.2214A>T | XP_011543871.1:p.Ala738= | |
| XM_011545570.1:c.2133A>T | XP_011543872.1:p.Ala711= | |
| XR_950484.1:n.2517A>T | ||
| NM_001323289.1:c.2265A>T | NP_001310218.1:p.Ala755= | |
| NM_001323289.2:c.2265A>T MANE Select | NP_001310218.1:p.Ala755= | |
| NM_001037343.2:c.2265A>T | NP_001032420.1:p.Ala755= | |
| NM_003159.3:c.2265A>T | NP_003150.1:p.Ala755= |