Linked Data
dbSNP Id:
rs576986850
gnomAD v2:
20-32026501-G-A
gnomAD v3:
20-33438695-G-A
gnomAD v4:
20-33438695-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.33438695G>A , CM000682.2:g.33438695G>A | GRCh38 |
| NC_000020.10:g.32026501G>A , CM000682.1:g.32026501G>A | GRCh37 |
| NC_000020.9:g.31490162G>A | NCBI36 |
| NG_011622.1:g.10198C>T , LRG_332:g.10198C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217381.3:c.496+146C>T MANE Select | ENSP00000217381.2:n.496+146C>T | |
| ENST00000217381.2:c.496+146C>T | ENSP00000217381.2:n.496+146C>T | |
| NM_003098.2:c.496+146C>T , LRG_332t1:c.496+146C>T | NP_003089.1:n.496+146C>T | |
| XM_005260517.1:c.496+146C>T | XP_005260574.1:n.496+146C>T | |
| XM_011529007.1:c.496+146C>T | XP_011527309.1:n.496+146C>T | |
| XM_011529008.1:c.496+146C>T | XP_011527310.1:n.496+146C>T | |
| XR_936612.1:n.729+146C>T | ||
| XM_024451971.1:c.169+146C>T | XP_024307739.1:n.169+146C>T | |
| NM_003098.3:c.496+146C>T MANE Select | NP_003089.1:n.496+146C>T |