Linked Data
ClinVar Variation Id:
156097
dbSNP Id:
rs267608421
gnomAD v4:
X-18510855-G-T
PubMed:
PMID:18790821
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.18510855G>T , CM000685.2:g.18510855G>T | GRCh38 |
| NC_000023.10:g.18528975G>T , CM000685.1:g.18528975G>T | GRCh37 |
| NC_000023.9:g.18438896G>T | NCBI36 |
| NG_008475.1:g.90251G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000623535.2:c.99+1G>T MANE Select | ENSP00000485244.1:n.99+1G>T | |
| ENST00000635828.1:c.99+1G>T | ENSP00000490170.1:n.99+1G>T | |
| ENST00000637881.1:c.99+1G>T | ENSP00000489879.1:n.99+1G>T | |
| ENST00000674046.1:c.99+1G>T | ENSP00000501174.1:n.99+1G>T | |
| ENST00000379989.6:c.99+1G>T | ENSP00000369325.3:n.99+1G>T | |
| ENST00000379996.7:c.99+1G>T | ENSP00000369332.3:n.99+1G>T | |
| ENST00000463994.4:c.99+1G>T | ENSP00000485184.1:n.99+1G>T | |
| ENST00000623364.3:c.99+1G>T | ENSP00000485581.1:n.99+1G>T | |
| ENST00000623535.1:c.99+1G>T | ENSP00000485244.1:n.99+1G>T | |
| ENST00000624700.3:c.99+1G>T | ENSP00000485359.1:n.99+1G>T | |
| NM_001037343.1:c.99+1G>T | NP_001032420.1:n.99+1G>T | |
| NM_003159.2:c.99+1G>T | NP_003150.1:n.99+1G>T | |
| XM_011545569.1:c.99+1G>T | XP_011543871.1:n.99+1G>T | |
| XM_011545570.1:c.13+1G>T | XP_011543872.1:n.13+1G>T | |
| XR_950484.1:n.351+1G>T | ||
| NM_001323289.1:c.99+1G>T | NP_001310218.1:n.99+1G>T | |
| NM_001323289.2:c.99+1G>T MANE Select | NP_001310218.1:n.99+1G>T | |
| NM_001037343.2:c.99+1G>T | NP_001032420.1:n.99+1G>T | |
| NM_003159.3:c.99+1G>T | NP_003150.1:n.99+1G>T |