Linked Data
ClinVar Variation Id:
2724978
ClinVar RCV Id:
RCV003518486
dbSNP Id:
rs1028043587
gnomAD v4:
19-33302349-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33302349G>A , CM000681.2:g.33302349G>A | GRCh38 |
| NC_000019.9:g.33793255G>A , CM000681.1:g.33793255G>A | GRCh37 |
| NC_000019.8:g.38485095G>A | NCBI36 |
| NG_012022.1:g.5176C>T , LRG_456:g.5176C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000498907.3:c.66C>T MANE Select | ENSP00000427514.1:p.Pro22= | |
| ENST00000498907.2:c.66C>T | ENSP00000427514.1:p.Pro22= | |
| NM_001285829.1:c.-292C>T | NP_001272758.1:n.-292C>T | |
| NM_001287424.1:c.171C>T | NP_001274353.1:p.Pro57= | |
| NM_001287435.1:c.24C>T | NP_001274364.1:p.Pro8= | |
| NM_004364.4:c.66C>T | NP_004355.2:p.Pro22= | |
| NM_001287424.2:c.171C>T | NP_001274353.1:p.Pro57= | |
| NM_004364.5:c.66C>T MANE Select | NP_004355.2:p.Pro22= | |
| NM_001285829.2:c.-292C>T | NP_001272758.1:n.-292C>T | |
| NM_001287435.2:c.24C>T | NP_001274364.1:p.Pro8= |