Linked Data
ClinVar Variation Id:
342479
ClinVar RCV Id:
RCV000284269
dbSNP Id:
rs142728549
gnomAD v2:
3-10194249-T-A
gnomAD v3:
3-10152565-T-A
gnomAD v4:
3-10152565-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10152565T>A , CM000665.2:g.10152565T>A | GRCh38 |
| NC_000003.11:g.10194249T>A , CM000665.1:g.10194249T>A | GRCh37 |
| NC_000003.10:g.10169249T>A | NCBI36 |
| NG_008212.3:g.15931T>A , LRG_322:g.15931T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696153.1:c.*2600T>A | ENSP00000512444.1:n.*2600T>A | |
| ENST00000256474.3:c.*2600T>A MANE Select | ENSP00000256474.3:n.*2600T>A | |
| NM_000551.3:c.*2600T>A , LRG_322t1:c.*2600T>A | NP_000542.1:n.*2600T>A | |
| NM_198156.2:c.*2600T>A | NP_937799.1:n.*2600T>A | |
| NM_001354723.1:c.*2796T>A | NP_001341652.1:n.*2796T>A | |
| NM_000551.4:c.*2600T>A MANE Select | NP_000542.1:n.*2600T>A | |
| NM_001354723.2:c.*2796T>A | NP_001341652.1:n.*2796T>A | |
| NM_198156.3:c.*2600T>A | NP_937799.1:n.*2600T>A |