Linked Data
dbSNP Id:
rs762639528
ExAC:
X:135741221 T / C
gnomAD v2:
X-135741221-T-C
gnomAD v4:
X-136659062-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659062T>C , CM000685.2:g.136659062T>C | GRCh38 |
| NC_000023.10:g.135741221T>C , CM000685.1:g.135741221T>C | GRCh37 |
| NC_000023.9:g.135568887T>C | NCBI36 |
| NG_007280.1:g.15886T>C , LRG_141:g.15886T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.*51T>C | ENSP00000512122.1:n.*51T>C | |
| ENST00000695725.1:c.180T>C | ENSP00000512123.1:p.Asp60= | |
| ENST00000695726.1:n.2401T>C | ||
| ENST00000695729.1:n.3236T>C | ||
| ENST00000370629.7:c.433T>C MANE Select | ENSP00000359663.2:p.Tyr145His | |
| ENST00000370628.2:c.370T>C | ENSP00000359662.2:p.Tyr124His | |
| ENST00000370629.6:c.433T>C | ENSP00000359663.2:p.Tyr145His | |
| NM_000074.2:c.433T>C , LRG_141t1:c.433T>C | NP_000065.1:p.Tyr145His | |
| NM_000074.3:c.433T>C MANE Select | NP_000065.1:p.Tyr145His |