Linked Data
ClinVar Variation Id:
2934009
ClinVar RCV Id:
RCV003795759
dbSNP Id:
rs1481390305
gnomAD v3:
X-25012915-C-T
gnomAD v4:
X-25012915-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25012915C>T , CM000685.2:g.25012915C>T | GRCh38 |
| NC_000023.10:g.25031032C>T , CM000685.1:g.25031032C>T | GRCh37 |
| NC_000023.9:g.24940953C>T | NCBI36 |
| NG_008281.1:g.8034G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.1073+7G>A MANE Select | ENSP00000368332.4:n.1073+7G>A | |
| ENST00000379044.4:c.1073+7G>A | ENSP00000368332.4:n.1073+7G>A | |
| NM_139058.2:c.1073+7G>A | NP_620689.1:n.1073+7G>A | |
| NM_139058.3:c.1073+7G>A MANE Select | NP_620689.1:n.1073+7G>A |