Linked Data
ClinVar Variation Id:
213446
dbSNP Id:
rs782395522
gnomAD v2:
X-153588757-T-C
gnomAD v4:
X-154360389-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154360389T>C , CM000685.2:g.154360389T>C | GRCh38 |
| NC_000023.10:g.153588757T>C , CM000685.1:g.153588757T>C | GRCh37 |
| NC_000023.9:g.153241951T>C | NCBI36 |
| NG_011506.1:g.19250A>G | |
| NG_011506.2:g.19250A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360319.9:c.3406A>G | ENSP00000353467.4:p.Ile1136Val | |
| ENST00000369850.10:c.3406A>G MANE Select | ENSP00000358866.3:p.Ile1136Val | |
| ENST00000369856.8:c.3325A>G | ENSP00000358872.4:p.Ile1109Val | |
| ENST00000422373.6:c.3160+966A>G | ENSP00000416926.2:n.3160+966A>G | |
| ENST00000610817.5:c.3463A>G | ENSP00000480593.2:n.3463A>G | |
| ENST00000673639.2:c.279+5047A>G | ||
| ENST00000676696.1:c.3685A>G | ENSP00000503392.1:n.3685A>G | |
| ENST00000344736.8:c.3406A>G | ENSP00000358863.3:p.Ile1136Val | |
| ENST00000360319.8:c.3406A>G | ENSP00000353467.4:p.Ile1136Val | |
| ENST00000369850.7:c.3406A>G | ENSP00000358866.3:p.Ile1136Val | |
| ENST00000369856.7:c.3325A>G | ENSP00000358872.4:p.Ile1109Val | |
| ENST00000420627.5:c.3362A>G | ENSP00000408921.1:n.3362A>G | |
| ENST00000422373.5:c.3406A>G | ENSP00000416926.1:p.Ile1136Val | |
| ENST00000610817.4:c.3325A>G | ENSP00000480593.1:p.Ile1109Val | |
| NM_001110556.1:c.3406A>G | NP_001104026.1:p.Ile1136Val | |
| NM_001456.3:c.3406A>G | NP_001447.2:p.Ile1136Val | |
| XM_011531127.1:c.3406A>G | XP_011529429.1:p.Ile1136Val | |
| XM_011531128.1:c.3406A>G | XP_011529430.1:p.Ile1136Val | |
| XM_011531129.1:c.3406A>G | XP_011529431.1:p.Ile1136Val | |
| XM_011531130.1:c.3406A>G | XP_011529432.1:p.Ile1136Val | |
| XM_011531131.1:c.3205A>G | XP_011529433.1:p.Ile1069Val | |
| NM_001110556.2:c.3406A>G MANE Select | NP_001104026.1:p.Ile1136Val | |
| NM_001456.4:c.3406A>G | NP_001447.2:p.Ile1136Val |