Linked Data
ClinVar Variation Id:
329573
dbSNP Id:
rs576104602
gnomAD v2:
19-46050700-T-C
gnomAD v3:
19-45547442-T-C
gnomAD v4:
19-45547442-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45547442T>C , CM000681.2:g.45547442T>C | GRCh38 |
| NC_000019.9:g.46050700T>C , CM000681.1:g.46050700T>C | GRCh37 |
| NC_000019.8:g.50742540T>C | NCBI36 |
| NG_013332.1:g.42423A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323060.4:c.143-17986A>G | ENSP00000319817.3:n.143-17986A>G | |
| ENST00000263275.5:c.*6072A>G MANE Select | ENSP00000263275.4:n.*6072A>G | |
| ENST00000263275.4:c.*6072A>G | ENSP00000263275.3:n.*6072A>G | |
| ENST00000323060.3:c.143-17986A>G | ENSP00000319817.3:n.143-17986A>G | |
| NM_001017989.2:c.143-17986A>G | NP_001017989.2:n.143-17986A>G | |
| NM_025136.3:c.*6072A>G | NP_079412.1:n.*6072A>G | |
| XM_011527348.1:c.-17-17986A>G | XP_011525650.1:n.-17-17986A>G | |
| NM_001017989.3:c.143-17986A>G | NP_001017989.2:n.143-17986A>G | |
| NM_025136.4:c.*6072A>G MANE Select | NP_079412.1:n.*6072A>G |