Linked Data
ClinVar Variation Id:
914182
ClinVar RCV Id:
RCV001168224
dbSNP Id:
rs910306671
gnomAD v2:
9-137735014-T-A
gnomAD v3:
9-134843168-T-A
gnomAD v4:
9-134843168-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134843168T>A , CM000671.2:g.134843168T>A | GRCh38 |
| NC_000009.11:g.137735014T>A , CM000671.1:g.137735014T>A | GRCh37 |
| NC_000009.10:g.136874835T>A | NCBI36 |
| NG_008030.1:g.206363T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371820.4:c.*865T>A | ENSP00000360885.4:n.*865T>A | |
| ENST00000371817.8:c.*865T>A MANE Select | ENSP00000360882.3:n.*865T>A | |
| ENST00000371817.7:c.*865T>A | ENSP00000360882.3:n.*865T>A | |
| ENST00000618395.4:c.*865T>A | ENSP00000481360.1:n.*865T>A | |
| NM_000093.4:c.*865T>A | NP_000084.3:n.*865T>A | |
| NM_001278074.1:c.*865T>A | NP_001265003.1:n.*865T>A | |
| NR_103451.2:n.71-22959A>T | ||
| NM_000093.5:c.*865T>A MANE Select | NP_000084.3:n.*865T>A |