Linked Data
ClinVar Variation Id:
15616
ClinVar RCV Id:
RCV000016883
dbSNP Id:
rs33978907
gnomAD v4:
11-5225488-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5225488A>T , CM000673.2:g.5225488A>T | GRCh38 |
| NC_000011.9:g.5246718A>T , CM000673.1:g.5246718A>T | GRCh37 |
| NC_000011.8:g.5203294A>T | NCBI36 |
| NG_000007.3:g.72128T>A | |
| NG_059281.1:g.6584T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647020.1:c.*110T>A | ENSP00000494175.1:n.*110T>A | |
| ENST00000335295.4:c.*110T>A MANE Select | ENSP00000333994.3:n.*110T>A | |
| ENST00000633227.1:c.*370T>A | ENSP00000488004.1:n.*370T>A | |
| NM_000518.4:c.*110T>A | NP_000509.1:n.*110T>A | |
| NM_000518.5:c.*110T>A MANE Select | NP_000509.1:n.*110T>A |