Linked Data
ClinVar Variation Id:
1100604
ClinVar RCV Id:
RCV001423243
dbSNP Id:
rs1772544155
gnomAD v4:
6-31962426-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31962426G>T , CM000668.2:g.31962426G>T | GRCh38 |
| NC_000006.11:g.31930203G>T , CM000668.1:g.31930203G>T | GRCh37 |
| NC_000006.10:g.32038182G>T | NCBI36 |
| NG_032652.1:g.8623G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461073.6:c.*181-13G>T | ENSP00000419905.1:n.*181-13G>T | |
| ENST00000483553.6:c.1065-13G>T | ENSP00000420332.2:n.1065-13G>T | |
| ENST00000485349.6:n.1106-13G>T | ||
| ENST00000491994.2:c.1065-13G>T | ENSP00000417586.2:n.1065-13G>T | |
| ENST00000494058.6:n.1122-13G>T | ||
| ENST00000697831.1:c.1065-13G>T | ENSP00000513453.1:n.1065-13G>T | |
| ENST00000697832.1:n.1141-13G>T | ||
| ENST00000697833.1:c.1065-13G>T | ENSP00000513454.1:n.1065-13G>T | |
| ENST00000697834.1:n.1117-13G>T | ||
| ENST00000697835.1:c.*583-13G>T | ENSP00000513455.1:n.*583-13G>T | |
| ENST00000697836.1:n.1101-13G>T | ||
| ENST00000697837.1:c.1065-13G>T | ENSP00000513456.1:n.1065-13G>T | |
| ENST00000697838.1:c.930-13G>T | ENSP00000513457.1:n.930-13G>T | |
| ENST00000697839.1:n.1348-13G>T | ||
| ENST00000697840.1:c.1101-13G>T | ENSP00000513458.1:n.1101-13G>T | |
| ENST00000697841.1:n.1637-13G>T | ||
| ENST00000697842.1:n.1065-13G>T | ||
| ENST00000375394.7:c.1065-13G>T MANE Select | ENSP00000364543.2:n.1065-13G>T | |
| ENST00000375394.6:c.1065-13G>T | ENSP00000364543.2:n.1065-13G>T | |
| ENST00000461073.5:c.*181-13G>T | ENSP00000419905.1:n.*181-13G>T | |
| ENST00000465703.5:n.1378-13G>T | ||
| ENST00000466290.1:n.326-13G>T | ||
| ENST00000474839.5:c.*437-13G>T | ENSP00000420470.1:n.*437-13G>T | |
| NM_006929.4:c.1065-13G>T | NP_008860.4:n.1065-13G>T | |
| XM_006715168.2:c.1065-13G>T | XP_006715231.1:n.1065-13G>T | |
| XM_011514815.1:c.1065-13G>T | XP_011513117.1:n.1065-13G>T | |
| XR_926301.1:n.1153-13G>T | ||
| XM_011514815.3:c.1065-13G>T | XP_011513117.1:n.1065-13G>T | |
| XR_001743586.2:n.1101-13G>T | ||
| XR_926301.3:n.1101-13G>T | ||
| NM_006929.5:c.1065-13G>T MANE Select | NP_008860.4:n.1065-13G>T |