Linked Data
ClinVar Variation Id:
1703261
ClinVar RCV Id:
RCV002280383
dbSNP Id:
rs4244285
gnomAD v4:
10-94781859-G-T
MyVariant Identifiers:
chr10:g.96541616G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94781859G>T , CM000672.2:g.94781859G>T | GRCh38 |
| NC_000010.10:g.96541616G>T , CM000672.1:g.96541616G>T | GRCh37 |
| NC_000010.9:g.96531606G>T | NCBI36 |
| NG_008384.2:g.24154G>T | |
| NG_008384.3:g.24179G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371321.9:c.681G>T MANE Select | ENSP00000360372.3:p.Pro227= | |
| ENST00000645461.1:n.1734G>T | ||
| ENST00000371321.7:c.681G>T | ENSP00000360372.3:p.Pro227= | |
| ENST00000464755.1:c.1444G>T | ENSP00000483243.1:n.1444G>T | |
| NM_000769.2:c.681G>T | NP_000760.1:p.Pro227= | |
| NM_000769.4:c.681G>T MANE Select | NP_000760.1:p.Pro227= |