Linked Data
ClinVar Variation Id:
1958471
ClinVar RCV Id:
RCV002696097
dbSNP Id:
rs560413403
gnomAD v4:
21-32657063-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.32657063G>C , CM000683.2:g.32657063G>C | GRCh38 |
| NC_000021.8:g.34029373G>C , CM000683.1:g.34029373G>C | GRCh37 |
| NC_000021.7:g.32951244G>C | NCBI36 |
| NG_030017.1:g.75979C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382499.7:c.2636C>G | ENSP00000371939.2:p.Thr879Arg | |
| ENST00000433931.7:c.2636C>G | ENSP00000409667.2:p.Thr879Arg | |
| ENST00000630077.3:c.2504C>G | ENSP00000487560.1:p.Thr835Arg | |
| ENST00000674204.1:c.2519C>G | ENSP00000501504.1:p.Thr840Arg | |
| ENST00000674308.1:c.2519C>G | ENSP00000501426.1:p.Thr840Arg | |
| ENST00000674351.1:c.2519C>G MANE Select | ENSP00000501530.1:p.Thr840Arg | |
| ENST00000357345.7:c.2519C>G | ENSP00000349903.3:p.Thr840Arg | |
| ENST00000382491.7:c.2504C>G | ENSP00000371931.4:p.Thr835Arg | |
| ENST00000382499.6:c.2636C>G | ENSP00000371939.2:p.Thr879Arg | |
| ENST00000433931.6:c.2636C>G | ENSP00000409667.2:p.Thr879Arg | |
| ENST00000464778.1:n.306C>G | ||
| ENST00000630077.2:c.2504C>G | ENSP00000487560.1:p.Thr835Arg | |
| NM_001160302.1:c.2519C>G | NP_001153774.1:p.Thr840Arg | |
| NM_001160306.1:c.2504C>G | NP_001153778.1:p.Thr835Arg | |
| NM_003895.3:c.2636C>G | NP_003886.3:p.Thr879Arg | |
| NM_203446.2:c.2636C>G | NP_982271.2:p.Thr879Arg | |
| XM_017028494.1:c.2519C>G | XP_016883983.1:p.Thr840Arg | |
| XM_017028495.2:c.2621C>G | XP_016883984.1:p.Thr874Arg | |
| XM_017028496.1:c.2519C>G | XP_016883985.1:p.Thr840Arg | |
| XM_017028497.2:c.2636C>G | XP_016883986.1:p.Thr879Arg | |
| XM_017028498.1:c.2519C>G | XP_016883987.1:p.Thr840Arg | |
| XM_017028499.2:c.2621C>G | XP_016883988.1:p.Thr874Arg | |
| XM_017028500.1:c.2519C>G | XP_016883989.1:p.Thr840Arg | |
| XM_017028501.1:c.2519C>G | XP_016883990.1:p.Thr840Arg | |
| XM_017028502.1:c.2519C>G | XP_016883991.1:p.Thr840Arg | |
| XM_017028503.1:c.2519C>G | XP_016883992.1:p.Thr840Arg | |
| XM_017028504.1:c.2519C>G | XP_016883993.1:p.Thr840Arg | |
| XM_017028505.2:c.2621C>G | XP_016883994.1:p.Thr874Arg | |
| NM_001160306.2:c.2504C>G | NP_001153778.1:p.Thr835Arg | |
| NM_203446.3:c.2519C>G MANE Select | NP_982271.3:p.Thr840Arg |