Linked Data
ClinVar Variation Id:
350924
dbSNP Id:
rs544519958
gnomAD v2:
5-136953721-G-A
gnomAD v3:
5-137618032-G-A
gnomAD v4:
5-137618032-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.137618032G>A , CM000667.2:g.137618032G>A | GRCh38 |
| NC_000005.9:g.136953721G>A , CM000667.1:g.136953721G>A | GRCh37 |
| NC_000005.8:g.136981620G>A | NCBI36 |
| NG_032569.1:g.123059C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309755.9:c.*4066C>T MANE Select | ENSP00000312397.4:n.*4066C>T | |
| ENST00000309755.8:c.*4066C>T | ENSP00000312397.4:n.*4066C>T | |
| ENST00000506491.5:c.*4066C>T | ENSP00000424828.1:n.*4066C>T | |
| ENST00000508657.5:c.*4066C>T | ENSP00000422099.1:n.*4066C>T | |
| ENST00000509694.1:n.623-168C>T | ||
| NM_001257194.1:c.*4066C>T | NP_001244123.1:n.*4066C>T | |
| NM_001257195.1:c.*4066C>T | NP_001244124.1:n.*4066C>T | |
| NM_017415.2:c.*4066C>T | NP_059111.2:n.*4066C>T | |
| NM_017415.3:c.*4066C>T MANE Select | NP_059111.2:n.*4066C>T | |
| NM_001257195.2:c.*4066C>T | NP_001244124.1:n.*4066C>T |