Linked Data
dbSNP Id:
rs775078060
ExAC:
1:173800714 T / G
gnomAD v2:
1-173800714-T-G
gnomAD v3:
1-173831576-T-G
gnomAD v4:
1-173831576-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.173831576T>G , CM000663.2:g.173831576T>G | GRCh38 |
| NC_000001.10:g.173800714T>G , CM000663.1:g.173800714T>G | GRCh37 |
| NC_000001.9:g.172067337T>G | NCBI36 |
| NG_016138.1:g.11918T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000471476.2:c.*128T>G | ENSP00000497663.1:n.*128T>G | |
| ENST00000647645.1:c.438T>G | ENSP00000497450.1:p.Ala146= | |
| ENST00000647730.1:c.*128T>G | ENSP00000497781.1:n.*128T>G | |
| ENST00000647788.1:c.*128T>G | ENSP00000497769.1:n.*128T>G | |
| ENST00000648271.1:c.*128T>G | ENSP00000497795.1:n.*128T>G | |
| ENST00000648458.1:c.438T>G | ENSP00000497874.1:p.Ala146= | |
| ENST00000648807.1:c.438T>G | ENSP00000497472.1:p.Ala146= | |
| ENST00000648960.1:c.438T>G | ENSP00000497091.1:p.Ala146= | |
| ENST00000649067.1:c.438T>G | ENSP00000497052.1:p.Ala146= | |
| ENST00000649689.2:c.438T>G MANE Select | ENSP00000497569.1:p.Ala146= | |
| ENST00000650297.1:n.821T>G | ||
| ENST00000361951.4:c.438T>G | ENSP00000355086.4:p.Ala146= | |
| NM_018122.4:c.438T>G | NP_060592.2:p.Ala146= | |
| XM_006711427.2:c.438T>G | XP_006711490.1:p.Ala146= | |
| XM_011509711.1:c.438T>G | XP_011508013.1:p.Ala146= | |
| NM_001365212.1:c.438T>G | NP_001352141.1:p.Ala146= | |
| NM_001365213.1:c.438T>G | NP_001352142.1:p.Ala146= | |
| NM_018122.5:c.438T>G MANE Select | NP_060592.2:p.Ala146= | |
| NM_001365213.2:c.438T>G | NP_001352142.1:p.Ala146= |