Linked Data
ClinVar Variation Id:
446666
dbSNP Id:
rs1553815019
gnomAD v4:
4-5574684-C-T
PubMed:
PMID:29068549
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.5574684C>T , CM000666.2:g.5574684C>T | GRCh38 |
| NC_000004.11:g.5576411C>T , CM000666.1:g.5576411C>T | GRCh37 |
| NC_000004.10:g.5627312C>T | NCBI36 |
| NG_015821.1:g.139865G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344408.10:c.3360+1G>A MANE Select | ENSP00000342144.5:n.3360+1G>A | |
| ENST00000310917.6:c.3120+1G>A | ENSP00000311683.2:n.3120+1G>A | |
| ENST00000344408.9:c.3360+1G>A | ENSP00000342144.5:n.3360+1G>A | |
| ENST00000475313.5:c.3120+1G>A | ENSP00000431981.1:n.3120+1G>A | |
| ENST00000509670.1:c.*1753+1G>A | ENSP00000423876.1:n.*1753+1G>A | |
| NM_001166136.1:c.3120+1G>A | NP_001159608.1:n.3120+1G>A | |
| NM_147127.4:c.3360+1G>A | NP_667338.3:n.3360+1G>A | |
| XM_011513392.1:c.3369+1G>A | XP_011511694.1:n.3369+1G>A | |
| XM_011513393.1:c.3369+1G>A | XP_011511695.1:n.3369+1G>A | |
| XM_011513394.1:c.3129+1G>A | XP_011511696.1:n.3129+1G>A | |
| XM_017007736.1:c.3120+1G>A | XP_016863225.1:n.3120+1G>A | |
| XM_017007737.1:c.3120+1G>A | XP_016863226.1:n.3120+1G>A | |
| XM_017007739.1:c.1680+1G>A | XP_016863228.1:n.1680+1G>A | |
| XM_024453893.1:c.1680+1G>A | XP_024309661.1:n.1680+1G>A | |
| XR_001741141.1:n.3210+1G>A | ||
| NM_147127.5:c.3360+1G>A MANE Select | NP_667338.3:n.3360+1G>A | |
| NM_001166136.2:c.3120+1G>A | NP_001159608.1:n.3120+1G>A |