Linked Data
dbSNP Id:
rs2011867492
gnomAD v3:
20-32436294-C-T
gnomAD v4:
20-32436294-C-T
MyVariant Identifiers:
chr20:g.31024097C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.32436294C>T , CM000682.2:g.32436294C>T | GRCh38 |
| NC_000020.10:g.31024097C>T , CM000682.1:g.31024097C>T | GRCh37 |
| NC_000020.9:g.30487758C>T | NCBI36 |
| NG_027868.1:g.82951C>T , LRG_630:g.82951C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375687.10:c.3582C>T MANE Select | ENSP00000364839.4:p.Thr1194= | |
| ENST00000646985.1:c.3399C>T | ENSP00000495053.1:p.Thr1133= | |
| ENST00000647223.1:n.5935C>T | ||
| ENST00000651418.1:c.1869+1713C>T | ENSP00000499150.1:n.1869+1713C>T | |
| ENST00000306058.9:c.3567C>T | ENSP00000305119.5:p.Thr1189= | |
| ENST00000375687.8:c.3582C>T | ENSP00000364839.4:p.Thr1194= | |
| ENST00000613218.4:c.3582C>T | ENSP00000480487.1:p.Thr1194= | |
| ENST00000620121.4:c.3582C>T | ENSP00000481978.1:p.Thr1194= | |
| NM_015338.5:c.3582C>T , LRG_630t1:c.3582C>T | NP_056153.2:p.Thr1194= | |
| XM_006723727.2:c.3579C>T | XP_006723790.1:p.Thr1193= | |
| XM_006723728.2:c.3552C>T | XP_006723791.1:p.Thr1184= | |
| XM_006723730.2:c.3498C>T | XP_006723793.1:p.Thr1166= | |
| XM_006723732.2:c.3399C>T | XP_006723795.1:p.Thr1133= | |
| XM_006723733.1:c.2898C>T | XP_006723796.1:p.Thr966= | |
| XM_011528647.1:c.3846C>T | XP_011526949.1:p.Thr1282= | |
| XM_011528648.1:c.3843C>T | XP_011526950.1:p.Thr1281= | |
| XM_011528649.1:c.3762C>T | XP_011526951.1:p.Thr1254= | |
| XM_011528650.1:c.3693C>T | XP_011526952.1:p.Thr1231= | |
| XM_011528651.1:c.3561C>T | XP_011526953.1:p.Thr1187= | |
| XM_011528652.1:c.3498C>T | XP_011526954.1:p.Thr1166= | |
| NM_001363734.1:c.3399C>T | NP_001350663.1:p.Thr1133= | |
| XM_006723727.3:c.3579C>T | XP_006723790.1:p.Thr1193= | |
| XM_006723728.3:c.3552C>T | XP_006723791.1:p.Thr1184= | |
| XM_006723730.4:c.3498C>T | XP_006723793.1:p.Thr1166= | |
| XM_011528648.3:c.3843C>T | XP_011526950.1:p.Thr1281= | |
| XM_011528652.2:c.3498C>T | XP_011526954.1:p.Thr1166= | |
| XM_017027704.1:c.3498C>T | XP_016883193.1:p.Thr1166= | |
| XM_017027705.1:c.3498C>T | XP_016883194.1:p.Thr1166= | |
| XM_017027706.1:c.3429C>T | XP_016883195.1:p.Thr1143= | |
| NM_015338.6:c.3582C>T MANE Select | NP_056153.2:p.Thr1194= |