Linked Data
dbSNP Id:
rs10849605
gnomAD v2:
12-1064438-T-C
gnomAD v3:
12-955272-T-C
gnomAD v4:
12-955272-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.955272T>C , CM000674.2:g.955272T>C | GRCh38 |
| NC_000012.11:g.1064438T>C , CM000674.1:g.1064438T>C | GRCh37 |
| NC_000012.10:g.934699T>C | NCBI36 |
| NG_017078.2:g.39770A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000430095.6:c.-18-22196A>G | ENSP00000387901.2:n.-18-22196A>G | |
| NM_001297419.1:c.-18-22196A>G | NP_001284348.1:n.-18-22196A>G | |
| XM_005253720.3:c.-18-22196A>G | XP_005253777.1:n.-18-22196A>G | |
| XM_005253720.5:c.-18-22196A>G | XP_005253777.1:n.-18-22196A>G | |
| XM_017019769.1:c.-18-22196A>G | XP_016875258.1:n.-18-22196A>G |