Linked Data
ClinVar Variation Id:
366699
dbSNP Id:
rs374014228
ExAC:
9:34648755 C / T
gnomAD v2:
9-34648755-C-T
gnomAD v3:
9-34648758-C-T
gnomAD v4:
9-34648758-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.34648758C>T , CM000671.2:g.34648758C>T | GRCh38 |
| NC_000009.11:g.34648755C>T , CM000671.1:g.34648755C>T | GRCh37 |
| NC_000009.10:g.34638755C>T | NCBI36 |
| NG_009029.1:g.7121C>T | |
| NG_028966.1:g.1574C>T | |
| NG_009029.2:g.7170C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000691183.1:c.*276-4C>T | ENSP00000509954.1:n.*276-4C>T | |
| ENST00000378842.8:c.688-4C>T MANE Select | ENSP00000368119.4:n.688-4C>T | |
| ENST00000378842.7:c.688-4C>T | ENSP00000368119.3:n.688-4C>T | |
| ENST00000450095.6:c.361-4C>T | ENSP00000401956.2:n.361-4C>T | |
| ENST00000473506.6:c.*276-4C>T | ENSP00000432839.2:n.*276-4C>T | |
| ENST00000473529.5:n.847-4C>T | ||
| ENST00000487381.5:n.1374C>T | ||
| ENST00000489643.6:n.764C>T | ||
| ENST00000554085.5:c.*432-4C>T | ENSP00000450419.1:n.*432-4C>T | |
| ENST00000554550.5:c.*308-4C>T | ENSP00000451435.1:n.*308-4C>T | |
| ENST00000554638.5:n.1160-4C>T | ||
| ENST00000555020.5:n.1145C>T | ||
| ENST00000555086.5:n.692-4C>T | ||
| ENST00000555754.1:n.33-4C>T | ||
| ENST00000556244.1:c.675-4C>T | ||
| ENST00000556278.1:c.432+302C>T | ENSP00000451792.1:n.432+302C>T | |
| ENST00000557706.5:n.1250-4C>T | ||
| NM_000155.3:c.688-4C>T | NP_000146.2:n.688-4C>T | |
| NM_001258332.1:c.361-4C>T | NP_001245261.1:n.361-4C>T | |
| NM_000155.4:c.688-4C>T MANE Select | NP_000146.2:n.688-4C>T | |
| NM_001258332.2:c.361-4C>T | NP_001245261.1:n.361-4C>T |