Linked Data
dbSNP Id:
rs757845380
ExAC:
2:207009722 C / T
gnomAD v2:
2-207009722-C-T
gnomAD v4:
2-206144998-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.206144998C>T , CM000664.2:g.206144998C>T | GRCh38 |
| NC_000002.11:g.207009722C>T , CM000664.1:g.207009722C>T | GRCh37 |
| NC_000002.10:g.206717967C>T | NCBI36 |
| NG_009248.1:g.19466G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233190.11:c.766G>A MANE Select | ENSP00000233190.5:p.Ala256Thr | |
| ENST00000233190.10:c.766G>A | ENSP00000233190.5:p.Ala256Thr | |
| ENST00000423725.5:c.595G>A | ENSP00000397760.1:p.Ala199Thr | |
| ENST00000432169.5:c.433G>A | ENSP00000409689.1:p.Ala145Thr | |
| ENST00000440274.5:c.658G>A | ENSP00000409766.1:p.Ala220Thr | |
| ENST00000449699.5:c.766G>A | ENSP00000399912.1:p.Ala256Thr | |
| ENST00000455934.6:c.808G>A | ENSP00000392709.2:p.Ala270Thr | |
| ENST00000457011.5:c.418G>A | ENSP00000400976.1:p.Ala140Thr | |
| NM_001199981.1:c.658G>A | NP_001186910.1:p.Ala220Thr | |
| NM_001199982.1:c.433G>A | NP_001186911.1:p.Ala145Thr | |
| NM_001199983.1:c.595G>A | NP_001186912.1:p.Ala199Thr | |
| NM_001199984.1:c.808G>A | NP_001186913.1:p.Ala270Thr | |
| NM_005006.6:c.766G>A | NP_004997.4:p.Ala256Thr | |
| XM_017004188.2:c.7G>A | XP_016859677.1:p.Ala3Thr | |
| NM_001199981.2:c.658G>A | NP_001186910.1:p.Ala220Thr | |
| NM_001199982.2:c.433G>A | NP_001186911.1:p.Ala145Thr | |
| NM_001199983.2:c.595G>A | NP_001186912.1:p.Ala199Thr | |
| NM_005006.7:c.766G>A MANE Select | NP_004997.4:p.Ala256Thr | |
| NM_001199984.2:c.808G>A | NP_001186913.1:p.Ala270Thr |