Linked Data
ClinVar Variation Id:
1027087
dbSNP Id:
rs1696261924
gnomAD v4:
3-10146538-C-T
CIViC:
CA351753771
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10146538C>T , CM000665.2:g.10146538C>T | GRCh38 |
| NC_000003.11:g.10188222C>T , CM000665.1:g.10188222C>T | GRCh37 |
| NC_000003.10:g.10163222C>T | NCBI36 |
| NG_008212.3:g.9904C>T , LRG_322:g.9904C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.*42C>T | ENSP00000512434.1:n.*42C>T | |
| ENST00000696143.1:c.600-3249C>T | ENSP00000512435.1:n.600-3249C>T | |
| ENST00000696153.1:c.365C>T | ENSP00000512444.1:p.Ala122Val | |
| ENST00000256474.3:c.365C>T MANE Select | ENSP00000256474.3:p.Ala122Val | |
| ENST00000256474.2:c.365C>T | ENSP00000256474.2:p.Ala122Val | |
| ENST00000345392.2:c.341-3249C>T | ENSP00000344757.2:n.341-3249C>T | |
| ENST00000477538.1:n.501C>T | ||
| NM_000551.3:c.365C>T , LRG_322t1:c.365C>T | NP_000542.1:p.Ala122Val | |
| NM_198156.2:c.341-3249C>T | NP_937799.1:n.341-3249C>T | |
| XM_011534078.1:c.*42C>T | XP_011532380.1:n.*42C>T | |
| NM_001354723.1:c.*18-3249C>T | NP_001341652.1:n.*18-3249C>T | |
| NM_000551.4:c.365C>T MANE Select | NP_000542.1:p.Ala122Val | |
| NM_001354723.2:c.*18-3249C>T | NP_001341652.1:n.*18-3249C>T | |
| NM_198156.3:c.341-3249C>T | NP_937799.1:n.341-3249C>T |