Linked Data
ClinVar Variation Id:
329555
dbSNP Id:
rs528812143
gnomAD v2:
19-46049870-C-T
gnomAD v3:
19-45546612-C-T
gnomAD v4:
19-45546612-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45546612C>T , CM000681.2:g.45546612C>T | GRCh38 |
| NC_000019.9:g.46049870C>T , CM000681.1:g.46049870C>T | GRCh37 |
| NC_000019.8:g.50741710C>T | NCBI36 |
| NG_013332.1:g.43253G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323060.4:c.143-17156G>A | ENSP00000319817.3:n.143-17156G>A | |
| ENST00000263275.5:c.*6902G>A MANE Select | ENSP00000263275.4:n.*6902G>A | |
| ENST00000263275.4:c.*6902G>A | ENSP00000263275.3:n.*6902G>A | |
| ENST00000323060.3:c.143-17156G>A | ENSP00000319817.3:n.143-17156G>A | |
| NM_001017989.2:c.143-17156G>A | NP_001017989.2:n.143-17156G>A | |
| NM_025136.3:c.*6902G>A | NP_079412.1:n.*6902G>A | |
| XM_011527348.1:c.-17-17156G>A | XP_011525650.1:n.-17-17156G>A | |
| NM_001017989.3:c.143-17156G>A | NP_001017989.2:n.143-17156G>A | |
| NM_025136.4:c.*6902G>A MANE Select | NP_079412.1:n.*6902G>A |