Linked Data
ClinVar Variation Id:
345582
dbSNP Id:
rs200207404
ExAC:
3:46937363 C / T
gnomAD v2:
3-46937363-C-T
gnomAD v3:
3-46895873-C-T
gnomAD v4:
3-46895873-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.46895873C>T , CM000665.2:g.46895873C>T | GRCh38 |
| NC_000003.11:g.46937363C>T , CM000665.1:g.46937363C>T | GRCh37 |
| NC_000003.10:g.46912367C>T | NCBI36 |
| NG_008864.1:g.23128C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000449590.6:c.313+4C>T MANE Select | ENSP00000402723.1:n.313+4C>T | |
| ENST00000313049.9:c.313+4C>T | ENSP00000321999.4:n.313+4C>T | |
| ENST00000418619.5:c.313+4C>T | ENSP00000411424.1:n.313+4C>T | |
| ENST00000427125.6:c.313+4C>T | ENSP00000400977.2:n.313+4C>T | |
| ENST00000428220.1:c.313+4C>T | ENSP00000389811.1:n.313+4C>T | |
| ENST00000430002.6:c.313+4C>T | ENSP00000413774.2:n.313+4C>T | |
| ENST00000449590.5:c.313+4C>T | ENSP00000402723.1:n.313+4C>T | |
| ENST00000490109.1:n.333+4C>T | ||
| NM_000316.2:c.313+4C>T | NP_000307.1:n.313+4C>T | |
| NM_001184744.1:c.313+4C>T | NP_001171673.1:n.313+4C>T | |
| XM_005265344.2:c.220+4C>T | XP_005265401.1:n.220+4C>T | |
| XM_011533967.1:c.352+4C>T | XP_011532269.1:n.352+4C>T | |
| XM_011533968.1:c.334+4C>T | XP_011532270.1:n.334+4C>T | |
| XM_005265344.3:c.220+4C>T | XP_005265401.1:n.220+4C>T | |
| XM_011533967.3:c.352+4C>T | XP_011532269.1:n.352+4C>T | |
| XM_011533968.2:c.334+4C>T | XP_011532270.1:n.334+4C>T | |
| XM_017006932.2:c.352+4C>T | XP_016862421.1:n.352+4C>T | |
| XM_017006933.1:c.313+4C>T | XP_016862422.1:n.313+4C>T | |
| XM_017006934.1:c.352+4C>T | XP_016862423.1:n.352+4C>T | |
| NM_000316.3:c.313+4C>T MANE Select | NP_000307.1:n.313+4C>T |