Linked Data
ClinVar Variation Id:
1953096
ClinVar RCV Id:
RCV002672219
dbSNP Id:
rs1166297442
gnomAD v2:
1-2337915-C-T
gnomAD v4:
1-2406476-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.2406476C>T , CM000663.2:g.2406476C>T | GRCh38 |
| NC_000001.10:g.2337915C>T , CM000663.1:g.2337915C>T | GRCh37 |
| NC_000001.9:g.2327775C>T | NCBI36 |
| NG_008342.1:g.11096G>A | |
| NG_016128.1:g.19702C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000288774.8:c.972+8G>A | ENSP00000288774.3:n.972+8G>A | |
| ENST00000447513.7:c.912+8G>A MANE Select | ENSP00000407922.2:n.912+8G>A | |
| ENST00000650293.1:c.866+8G>A | ||
| ENST00000288774.7:c.972+8G>A | ENSP00000288774.3:n.972+8G>A | |
| ENST00000447513.6:c.912+8G>A | ENSP00000407922.2:n.912+8G>A | |
| ENST00000507596.5:c.912+8G>A | ENSP00000424291.1:n.912+8G>A | |
| NM_002617.3:c.912+8G>A | NP_002608.1:n.912+8G>A | |
| NM_153818.1:c.972+8G>A | NP_722540.1:n.972+8G>A | |
| XM_011541573.1:c.969+8G>A | XP_011539875.1:n.969+8G>A | |
| XM_011541574.1:c.537+8G>A | XP_011539876.1:n.537+8G>A | |
| XM_011541575.1:c.537+8G>A | XP_011539877.1:n.537+8G>A | |
| XR_946666.1:n.1028+8G>A | ||
| XR_946666.2:n.977+8G>A | ||
| NM_001374425.1:c.969+8G>A | NP_001361354.1:n.969+8G>A | |
| NM_001374426.1:c.537+8G>A | NP_001361355.1:n.537+8G>A | |
| NM_001374427.1:c.480+8G>A | NP_001361356.1:n.480+8G>A | |
| NM_002617.4:c.912+8G>A MANE Select | NP_002608.1:n.912+8G>A | |
| NM_153818.2:c.972+8G>A | NP_722540.1:n.972+8G>A | |
| NR_164636.1:n.1027+8G>A |