Linked Data
ClinVar Variation Id:
2966645
ClinVar RCV Id:
RCV003828779
dbSNP Id:
rs916954732
gnomAD v4:
4-1003483-C-T
MyVariant Identifiers:
chr4:g.1003483C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.1003483C>T , CM000666.2:g.1003483C>T | GRCh38 |
| NC_000004.11:g.997271C>T , CM000666.1:g.997271C>T | GRCh37 |
| NC_000004.10:g.987271C>T | NCBI36 |
| NG_008103.1:g.21487C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000247933.9:c.1650+13C>T | ENSP00000247933.4:n.1650+13C>T | |
| ENST00000514224.2:c.1650+13C>T MANE Select | ENSP00000425081.2:n.1650+13C>T | |
| ENST00000652070.1:n.1706+13C>T | ||
| ENST00000247933.8:c.1650+13C>T | ENSP00000247933.4:n.1650+13C>T | |
| ENST00000514224.1:c.1254+13C>T | ENSP00000425081.1:n.1254+13C>T | |
| ENST00000514417.1:n.42+13C>T | ||
| ENST00000514698.5:n.1757+13C>T | ||
| NM_000203.4:c.1650+13C>T | NP_000194.2:n.1650+13C>T | |
| NR_110313.1:n.1738+13C>T | ||
| XM_006713882.2:c.1254+13C>T | XP_006713945.1:n.1254+13C>T | |
| XM_011513459.1:c.1716+13C>T | XP_011511761.1:n.1716+13C>T | |
| XM_011513460.1:c.1509+13C>T | XP_011511762.1:n.1509+13C>T | |
| XM_011513461.1:c.1443+13C>T | XP_011511763.1:n.1443+13C>T | |
| XM_011513462.1:c.1362+13C>T | XP_011511764.1:n.1362+13C>T | |
| XM_011513463.1:c.1362+13C>T | XP_011511765.1:n.1362+13C>T | |
| XR_924947.1:n.1906+13C>T | ||
| NM_000203.5:c.1650+13C>T MANE Select | NP_000194.2:n.1650+13C>T | |
| NM_001363576.1:c.1254+13C>T | NP_001350505.1:n.1254+13C>T | |
| XM_011513461.2:c.1443+13C>T | XP_011511763.1:n.1443+13C>T | |
| XM_017008163.1:c.690+13C>T | XP_016863652.1:n.690+13C>T |