Linked Data
dbSNP Id:
rs10488854
gnomAD v2:
4-72624135-C-T
gnomAD v3:
4-71758418-C-T
gnomAD v4:
4-71758418-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.71758418C>T , CM000666.2:g.71758418C>T | GRCh38 |
| NC_000004.11:g.72624135C>T , CM000666.1:g.72624135C>T | GRCh37 |
| NC_000004.10:g.72842999C>T | NCBI36 |
| NG_012837.2:g.52103G>A | |
| NG_012837.3:g.52103G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000273951.13:c.702-247G>A MANE Select | ENSP00000273951.8:n.702-247G>A | |
| ENST00000273951.12:c.702-247G>A | ENSP00000273951.8:n.702-247G>A | |
| ENST00000503472.5:n.586-247G>A | ||
| ENST00000504199.5:c.759-247G>A | ENSP00000421725.1:n.759-247G>A | |
| ENST00000509740.5:c.702-247G>A | ENSP00000422664.1:n.702-247G>A | |
| ENST00000513476.5:c.702-247G>A | ENSP00000426683.1:n.702-247G>A | |
| NM_000583.3:c.702-247G>A | NP_000574.2:n.702-247G>A | |
| NM_001204306.1:c.702-247G>A | NP_001191235.1:n.702-247G>A | |
| NM_001204307.1:c.759-247G>A | NP_001191236.1:n.759-247G>A | |
| XM_006714177.2:c.702-247G>A | XP_006714240.1:n.702-247G>A | |
| XM_006714177.3:c.702-247G>A | XP_006714240.1:n.702-247G>A | |
| NM_000583.4:c.702-247G>A MANE Select | NP_000574.2:n.702-247G>A |