Linked Data
ClinVar Variation Id:
1552554
ClinVar RCV Id:
RCV002197050
dbSNP Id:
rs2147315564
gnomAD v4:
X-38352781-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38352781A>G , CM000685.2:g.38352781A>G | GRCh38 |
| NC_000023.10:g.38212034A>G , CM000685.1:g.38212034A>G | GRCh37 |
| NC_000023.9:g.38096978A>G | NCBI36 |
| NG_008471.1:g.5299A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.77+8A>G MANE Select | ENSP00000039007.4:n.77+8A>G | |
| ENST00000643344.1:c.77+8A>G | ENSP00000496606.1:n.77+8A>G | |
| ENST00000039007.4:c.77+8A>G | ENSP00000039007.4:n.77+8A>G | |
| ENST00000465127.1:c.172-313340A>G | ENSP00000417050.1:n.172-313340A>G | |
| ENST00000488812.1:n.169+8A>G | ||
| NM_000531.5:c.77+8A>G | NP_000522.3:n.77+8A>G | |
| XM_017029556.1:c.77+8A>G | XP_016885045.1:n.77+8A>G | |
| NM_000531.6:c.77+8A>G MANE Select | NP_000522.3:n.77+8A>G |