Linked Data
ClinVar Variation Id:
156619
ClinVar RCV Id:
RCV000144762
dbSNP Id:
rs587783096
gnomAD v4:
X-25007418-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25007418C>T , CM000685.2:g.25007418C>T | GRCh38 |
| NC_000023.10:g.25025535C>T , CM000685.1:g.25025535C>T | GRCh37 |
| NC_000023.9:g.24935456C>T | NCBI36 |
| NG_008281.1:g.13531G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000379044.5:c.1141G>A MANE Select | ENSP00000368332.4:p.Ala381Thr | |
| ENST00000379044.4:c.1141G>A | ENSP00000368332.4:p.Ala381Thr | |
| NM_139058.2:c.1141G>A | NP_620689.1:p.Ala381Thr | |
| NM_139058.3:c.1141G>A MANE Select | NP_620689.1:p.Ala381Thr |