Linked Data
ClinVar Variation Id:
214183
dbSNP Id:
rs863223919
gnomAD v2:
10-102748934-C-T
gnomAD v4:
10-100989177-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.100989177C>T , CM000672.2:g.100989177C>T | GRCh38 |
| NC_000010.10:g.102748934C>T , CM000672.1:g.102748934C>T | GRCh37 |
| NC_000010.9:g.102738924C>T | NCBI36 |
| NG_011646.1:g.3339G>A | |
| NG_012624.1:g.6642C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311916.8:c.967C>T MANE Select | ENSP00000309595.2:p.Arg323Ter | |
| ENST00000370228.2:c.967C>T | ENSP00000359248.1:p.Arg323Ter | |
| ENST00000643860.1:c.967C>T | ENSP00000494389.1:p.Arg323Ter | |
| ENST00000646226.1:n.59-467C>T | ||
| ENST00000311916.6:c.967C>T | ENSP00000309595.2:p.Arg323Ter | |
| ENST00000370228.1:c.967C>T | ENSP00000359248.1:p.Arg323Ter | |
| ENST00000459764.1:n.87-467C>T | ||
| ENST00000473656.5:n.65-467C>T | ||
| ENST00000476766.5:n.192-529C>T | ||
| NM_001163812.1:c.967C>T | NP_001157284.1:p.Arg323Ter | |
| NM_001163813.1:c.-119-467C>T | NP_001157285.1:n.-119-467C>T | |
| NM_001163814.1:c.-119-467C>T | NP_001157286.1:n.-119-467C>T | |
| NM_021830.4:c.967C>T | NP_068602.2:p.Arg323Ter | |
| XM_011539975.1:c.-57-529C>T | XP_011538277.1:n.-57-529C>T | |
| XR_945788.1:n.1800C>T | ||
| XM_011539975.2:c.-57-529C>T | XP_011538277.1:n.-57-529C>T | |
| XM_017016437.1:c.-334C>T | XP_016871926.1:n.-334C>T | |
| XR_001747142.1:n.1141C>T | ||
| XR_001747144.1:n.1141C>T | ||
| XR_002956991.1:n.1141C>T | ||
| XR_945788.2:n.1141C>T | ||
| NM_021830.5:c.967C>T MANE Select | NP_068602.2:p.Arg323Ter | |
| NM_001163812.2:c.967C>T | NP_001157284.1:p.Arg323Ter | |
| NM_001163813.2:c.-119-467C>T | NP_001157285.1:n.-119-467C>T | |
| NM_001163814.2:c.-119-467C>T | NP_001157286.1:n.-119-467C>T | |
| NM_001368275.1:c.-57-529C>T | NP_001355204.1:n.-57-529C>T | |
| NR_160738.1:n.1635C>T | ||
| NR_160739.1:n.72-467C>T | ||
| NR_160740.1:n.1635C>T | ||
| NR_160741.1:n.1635C>T | ||
| NR_160742.1:n.1635C>T |