Linked Data
ClinVar Variation Id:
799716
dbSNP Id:
rs1458491740
gnomAD v4:
1-21570343-C-T
MyVariant Identifiers:
chr1:g.21896836C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.21570343C>T , CM000663.2:g.21570343C>T | GRCh38 |
| NC_000001.10:g.21896836C>T , CM000663.1:g.21896836C>T | GRCh37 |
| NC_000001.9:g.21769423C>T | NCBI36 |
| NG_008940.1:g.65979C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374840.8:c.831C>T MANE Select | ENSP00000363973.3:p.Thr277= | |
| ENST00000374830.2:c.41C>T | ||
| ENST00000374832.5:c.831C>T | ENSP00000363965.1:p.Thr277= | |
| ENST00000374840.7:c.831C>T | ENSP00000363973.3:p.Thr277= | |
| ENST00000539907.5:c.600C>T | ENSP00000437674.1:p.Thr200= | |
| ENST00000540617.5:c.666C>T | ENSP00000442672.1:p.Thr222= | |
| NM_000478.4:c.831C>T | NP_000469.3:p.Thr277= | |
| NM_001127501.2:c.666C>T | NP_001120973.2:p.Thr222= | |
| NM_001177520.1:c.600C>T | NP_001170991.1:p.Thr200= | |
| XM_005245818.1:c.831C>T | XP_005245875.1:p.Thr277= | |
| XM_005245820.2:c.831C>T | XP_005245877.1:p.Thr277= | |
| XM_006710546.1:c.831C>T | XP_006710609.1:p.Thr277= | |
| NM_000478.5:c.831C>T | NP_000469.3:p.Thr277= | |
| NM_001127501.3:c.666C>T | NP_001120973.2:p.Thr222= | |
| NM_001177520.2:c.600C>T | NP_001170991.1:p.Thr200= | |
| XM_006710546.3:c.831C>T | XP_006710609.1:p.Thr277= | |
| XM_017000903.1:c.675C>T | XP_016856392.1:p.Thr225= | |
| NM_000478.6:c.831C>T MANE Select | NP_000469.3:p.Thr277= | |
| NM_001127501.4:c.666C>T | NP_001120973.2:p.Thr222= | |
| NM_001177520.3:c.600C>T | NP_001170991.1:p.Thr200= | |
| NM_001369803.2:c.831C>T | NP_001356732.1:p.Thr277= | |
| NM_001369804.2:c.831C>T | NP_001356733.1:p.Thr277= | |
| NM_001369805.2:c.831C>T | NP_001356734.1:p.Thr277= |