Linked Data
ClinVar Variation Id:
264534
dbSNP Id:
rs200615848
ExAC:
X:153587999 T / C
gnomAD v2:
X-153587999-T-C
gnomAD v3:
X-154359631-T-C
gnomAD v4:
X-154359631-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154359631T>C , CM000685.2:g.154359631T>C | GRCh38 |
| NC_000023.10:g.153587999T>C , CM000685.1:g.153587999T>C | GRCh37 |
| NC_000023.9:g.153241193T>C | NCBI36 |
| NG_011506.1:g.20008A>G | |
| NG_011506.2:g.20008A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360319.9:c.3995A>G | ENSP00000353467.4:p.Asp1332Gly | |
| ENST00000369850.10:c.3995A>G MANE Select | ENSP00000358866.3:p.Asp1332Gly | |
| ENST00000369856.8:c.3914A>G | ENSP00000358872.4:p.Asp1305Gly | |
| ENST00000422373.6:c.3160+1724A>G | ENSP00000416926.2:n.3160+1724A>G | |
| ENST00000610817.5:c.4052A>G | ENSP00000480593.2:n.4052A>G | |
| ENST00000673639.2:c.279+5805A>G | ||
| ENST00000676696.1:c.4274A>G | ENSP00000503392.1:n.4274A>G | |
| ENST00000344736.8:c.3995A>G | ENSP00000358863.3:p.Asp1332Gly | |
| ENST00000360319.8:c.3995A>G | ENSP00000353467.4:p.Asp1332Gly | |
| ENST00000369850.7:c.3995A>G | ENSP00000358866.3:p.Asp1332Gly | |
| ENST00000369856.7:c.3914A>G | ENSP00000358872.4:p.Asp1305Gly | |
| ENST00000420627.5:c.3951A>G | ENSP00000408921.1:n.3951A>G | |
| ENST00000422373.5:c.3995A>G | ENSP00000416926.1:p.Asp1332Gly | |
| ENST00000490936.5:n.8A>G | ||
| ENST00000610817.4:c.3914A>G | ENSP00000480593.1:p.Asp1305Gly | |
| NM_001110556.1:c.3995A>G | NP_001104026.1:p.Asp1332Gly | |
| NM_001456.3:c.3995A>G | NP_001447.2:p.Asp1332Gly | |
| XM_011531127.1:c.3995A>G | XP_011529429.1:p.Asp1332Gly | |
| XM_011531128.1:c.3995A>G | XP_011529430.1:p.Asp1332Gly | |
| XM_011531129.1:c.3995A>G | XP_011529431.1:p.Asp1332Gly | |
| XM_011531130.1:c.3995A>G | XP_011529432.1:p.Asp1332Gly | |
| XM_011531131.1:c.3794A>G | XP_011529433.1:p.Asp1265Gly | |
| NM_001110556.2:c.3995A>G MANE Select | NP_001104026.1:p.Asp1332Gly | |
| NM_001456.4:c.3995A>G | NP_001447.2:p.Asp1332Gly |