Linked Data
ClinVar Variation Id:
334583
ClinVar RCV Id:
RCV000289627
dbSNP Id:
rs886055681
gnomAD v3:
2-224471149-C-G
gnomAD v4:
2-224471149-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.224471149C>G , CM000664.2:g.224471149C>G | GRCh38 |
| NC_000002.11:g.225335866C>G , CM000664.1:g.225335866C>G | GRCh37 |
| NC_000002.10:g.225044110C>G | NCBI36 |
| NG_032169.1:g.119249G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264414.9:c.*3096G>C MANE Select | ENSP00000264414.4:n.*3096G>C | |
| ENST00000264414.8:c.*3096G>C | ENSP00000264414.4:n.*3096G>C | |
| ENST00000344951.8:c.*3096G>C | ENSP00000343601.4:n.*3096G>C | |
| NM_001257197.1:c.*3096G>C | NP_001244126.1:n.*3096G>C | |
| NM_001257198.1:c.*3096G>C | NP_001244127.1:n.*3096G>C | |
| NM_003590.4:c.*3096G>C | NP_003581.1:n.*3096G>C | |
| NM_003590.5:c.*3096G>C MANE Select | NP_003581.1:n.*3096G>C | |
| NM_001257198.2:c.*3096G>C | NP_001244127.1:n.*3096G>C | |
| NM_001257197.2:c.*3096G>C | NP_001244126.1:n.*3096G>C |