Linked Data
ClinVar Variation Id:
827325
ClinVar RCV Id:
RCV001026943
dbSNP Id:
rs1450949342
gnomAD v2:
13-32905164-C-T
gnomAD v3:
13-32331027-C-T
gnomAD v4:
13-32331027-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32331027C>T , CM000675.2:g.32331027C>T | GRCh38 |
| NC_000013.10:g.32905164C>T , CM000675.1:g.32905164C>T | GRCh37 |
| NC_000013.9:g.31803164C>T | NCBI36 |
| NG_012772.3:g.20548C>T , LRG_293:g.20548C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000470094.2:c.790C>T | ENSP00000434898.2:p.His264Tyr | |
| ENST00000528762.2:c.790C>T | ENSP00000433168.2:p.His264Tyr | |
| ENST00000530893.7:c.421C>T | ENSP00000499438.2:p.His141Tyr | |
| ENST00000665585.2:c.790C>T | ENSP00000499570.2:p.His264Tyr | |
| ENST00000666593.2:c.790C>T | ENSP00000499256.2:p.His264Tyr | |
| ENST00000700202.2:c.790C>T | ENSP00000514856.2:p.His264Tyr | |
| ENST00000700201.1:c.*569C>T | ENSP00000514855.1:n.*569C>T | |
| ENST00000380152.8:c.790C>T MANE Select | ENSP00000369497.3:p.His264Tyr | |
| ENST00000544455.6:c.790C>T | ENSP00000439902.1:p.His264Tyr | |
| ENST00000614259.2:c.790C>T | ENSP00000506251.1:p.His264Tyr | |
| ENST00000680887.1:c.790C>T | ENSP00000505508.1:p.His264Tyr | |
| ENST00000380152.7:c.790C>T | ENSP00000369497.3:p.His264Tyr | |
| ENST00000530893.6:n.988C>T | ||
| ENST00000544455.5:c.790C>T | ENSP00000439902.1:p.His264Tyr | |
| ENST00000614259.1:n.790C>T | ||
| NM_000059.3:c.790C>T , LRG_293t1:c.790C>T | NP_000050.2:p.His264Tyr | |
| XM_011535203.1:c.790C>T | XP_011533505.1:p.His264Tyr | |
| XM_011535204.1:c.790C>T | XP_011533506.1:p.His264Tyr | |
| XM_011535205.1:c.790C>T | XP_011533507.1:p.His264Tyr | |
| NM_000059.4:c.790C>T MANE Select | NP_000050.3:p.His264Tyr |