Linked Data
dbSNP Id:
rs1342877038
gnomAD v2:
8-82390887-T-C
gnomAD v3:
8-81478652-T-C
gnomAD v4:
8-81478652-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.81478652T>C , CM000670.2:g.81478652T>C | GRCh38 |
| NC_000008.10:g.82390887T>C , CM000670.1:g.82390887T>C | GRCh37 |
| NC_000008.9:g.82553442T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256104.5:c.*213A>G MANE Select | ENSP00000256104.4:n.*213A>G | |
| ENST00000256104.4:c.*213A>G | ENSP00000256104.4:n.*213A>G | |
| NM_001442.2:c.*213A>G | NP_001433.1:n.*213A>G | |
| XR_001745980.1:n.514+16678T>C | ||
| NM_001442.3:c.*213A>G MANE Select | NP_001433.1:n.*213A>G |