Linked Data
ClinVar Variation Id:
128430
dbSNP Id:
rs538199862
ExAC:
20:47580444 C / T
gnomAD v2:
20-47580444-C-T
gnomAD v3:
20-48963907-C-T
gnomAD v4:
20-48963907-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.48963907C>T , CM000682.2:g.48963907C>T | GRCh38 |
| NC_000020.10:g.47580444C>T , CM000682.1:g.47580444C>T | GRCh37 |
| NC_000020.9:g.47013851C>T | NCBI36 |
| NG_011490.1:g.47170C>T | |
| NG_011490.2:g.47170C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371917.5:c.907+9C>T MANE Select | ENSP00000360985.4:n.907+9C>T | |
| ENST00000679436.1:c.907+9C>T | ENSP00000504888.1:n.907+9C>T | |
| ENST00000679542.1:n.464+9C>T | ||
| ENST00000680635.1:n.464+9C>T | ||
| ENST00000680871.1:c.907+9C>T | ENSP00000505042.1:n.907+9C>T | |
| ENST00000681021.1:c.907+9C>T | ENSP00000505972.1:n.907+9C>T | |
| ENST00000681399.1:c.*590+9C>T | ENSP00000506363.1:n.*590+9C>T | |
| ENST00000681656.1:c.907+9C>T | ENSP00000505638.1:n.907+9C>T | |
| ENST00000681885.1:c.907+9C>T | ENSP00000505737.1:n.907+9C>T | |
| ENST00000371917.4:c.907+9C>T | ENSP00000360985.4:n.907+9C>T | |
| NM_006420.2:c.907+9C>T | NP_006411.2:n.907+9C>T | |
| XM_005260252.2:c.907+9C>T | XP_005260309.1:n.907+9C>T | |
| XM_005260252.3:c.907+9C>T | XP_005260309.1:n.907+9C>T | |
| NM_006420.3:c.907+9C>T MANE Select | NP_006411.2:n.907+9C>T |