Linked Data
ClinVar Variation Id:
1366341
ClinVar RCV Id:
RCV001944633
dbSNP Id:
rs1344497909
gnomAD v4:
4-186208952-C-T
COSMIC:
COSM1173043
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186208952C>T , CM000666.2:g.186208952C>T | GRCh38 |
| NC_000004.11:g.187130106C>T , CM000666.1:g.187130106C>T | GRCh37 |
| NC_000004.10:g.187367100C>T | NCBI36 |
| NG_007965.1:g.22433C>T | |
| NG_012095.2:g.4974C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378802.5:c.1178C>T MANE Select | ENSP00000368079.4:p.Pro393Leu | |
| ENST00000378802.4:c.1178C>T | ENSP00000368079.4:p.Pro393Leu | |
| ENST00000502665.1:n.413C>T | ||
| ENST00000507209.5:n.5876C>T | ||
| ENST00000513354.5:n.268C>T | ||
| NM_207352.3:c.1178C>T | NP_997235.3:p.Pro393Leu | |
| XM_005262935.2:c.1178C>T | XP_005262992.1:p.Pro393Leu | |
| XM_006714184.2:c.782C>T | XP_006714247.1:p.Pro261Leu | |
| XM_005262935.4:c.1178C>T | XP_005262992.1:p.Pro393Leu | |
| XM_017008037.1:c.782C>T | XP_016863526.1:p.Pro261Leu | |
| NM_207352.4:c.1178C>T MANE Select | NP_997235.3:p.Pro393Leu |