Linked Data
ClinVar Variation Id:
11188
ClinVar RCV Id:
RCV000011939
dbSNP Id:
rs104894743
gnomAD v4:
X-25012937-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25012937G>A , CM000685.2:g.25012937G>A | GRCh38 |
| NC_000023.10:g.25031054G>A , CM000685.1:g.25031054G>A | GRCh37 |
| NC_000023.9:g.24940975G>A | NCBI36 |
| NG_008281.1:g.8012C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000379044.5:c.1058C>T MANE Select | ENSP00000368332.4:p.Pro353Leu | |
| ENST00000379044.4:c.1058C>T | ENSP00000368332.4:p.Pro353Leu | |
| NM_139058.2:c.1058C>T | NP_620689.1:p.Pro353Leu | |
| NM_139058.3:c.1058C>T MANE Select | NP_620689.1:p.Pro353Leu |