Linked Data
ClinVar Variation Id:
2186242
ClinVar RCV Id:
RCV002606488
dbSNP Id:
rs1762521736
gnomAD v4:
6-1610754-C-T
MyVariant Identifiers:
chr6:g.1610989C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1610754C>T , CM000668.2:g.1610754C>T | GRCh38 |
| NC_000006.11:g.1610989C>T , CM000668.1:g.1610989C>T | GRCh37 |
| NC_000006.10:g.1555988C>T | NCBI36 |
| NG_009368.1:g.5309C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.309C>T MANE Select | ENSP00000493906.1:p.Gly103= | |
| ENST00000380874.3:c.309C>T | ENSP00000370256.2:p.Gly103= | |
| NM_001453.2:c.309C>T | NP_001444.2:p.Gly103= | |
| NM_001453.3:c.309C>T MANE Select | NP_001444.2:p.Gly103= |