Linked Data
ClinVar Variation Id:
1589041
ClinVar RCV Id:
RCV002117178
dbSNP Id:
rs939761498
gnomAD v4:
8-38146151-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38146151C>T , CM000670.2:g.38146151C>T | GRCh38 |
| NC_000008.10:g.38003669C>T , CM000670.1:g.38003669C>T | GRCh37 |
| NC_000008.9:g.38122826C>T | NCBI36 |
| NG_011827.1:g.9932G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000276449.9:c.466-4G>A MANE Select | ENSP00000276449.3:n.466-4G>A | |
| ENST00000276449.8:c.466-4G>A | ENSP00000276449.3:n.466-4G>A | |
| ENST00000520114.1:n.953-4G>A | ||
| ENST00000522050.1:c.402-4G>A | ||
| NM_000349.2:c.466-4G>A | NP_000340.2:n.466-4G>A | |
| XM_006716392.1:c.466-4G>A | XP_006716455.1:n.466-4G>A | |
| NM_000349.3:c.466-4G>A MANE Select | NP_000340.2:n.466-4G>A |