Linked Data
ClinVar Variation Id:
345317
ClinVar RCV Id:
RCV000343535
dbSNP Id:
rs141957829
ExAC:
3:4459813 C / T
gnomAD v2:
3-4459813-C-T
gnomAD v3:
3-4418129-C-T
gnomAD v4:
3-4418129-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.4418129C>T , CM000665.2:g.4418129C>T | GRCh38 |
| NC_000003.11:g.4459813C>T , CM000665.1:g.4459813C>T | GRCh37 |
| NC_000003.10:g.4434813C>T | NCBI36 |
| NG_016225.1:g.54154G>A | |
| NG_016225.2:g.54154G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272902.10:c.606G>A MANE Select | ENSP00000272902.5:p.Pro202= | |
| ENST00000272902.9:c.606G>A | ENSP00000272902.5:p.Pro202= | |
| ENST00000383843.9:c.531G>A | ENSP00000373355.5:p.Pro177= | |
| ENST00000405420.2:c.606G>A | ENSP00000384977.2:p.Pro202= | |
| ENST00000448413.5:c.606G>A | ENSP00000404384.1:p.Pro202= | |
| ENST00000458465.6:c.445-7151G>A | ENSP00000410060.2:n.445-7151G>A | |
| NM_001164674.1:c.531G>A | NP_001158146.1:p.Pro177= | |
| NM_001164675.1:c.606G>A | NP_001158147.1:p.Pro202= | |
| NM_182760.3:c.606G>A | NP_877437.2:p.Pro202= | |
| XM_011533623.1:c.606G>A | XP_011531925.1:p.Pro202= | |
| XM_011533624.1:c.606G>A | XP_011531926.1:p.Pro202= | |
| XM_011533625.1:c.606G>A | XP_011531927.1:p.Pro202= | |
| XM_011533626.1:c.606G>A | XP_011531928.1:p.Pro202= | |
| XM_011533624.3:c.606G>A | XP_011531926.1:p.Pro202= | |
| XM_011533625.3:c.606G>A | XP_011531927.1:p.Pro202= | |
| XM_011533626.3:c.606G>A | XP_011531928.1:p.Pro202= | |
| XM_017006252.2:c.606G>A | XP_016861741.1:p.Pro202= | |
| XM_017006253.1:c.531G>A | XP_016861742.1:p.Pro177= | |
| XM_017006254.2:c.606G>A | XP_016861743.1:p.Pro202= | |
| XM_017006255.2:c.606G>A | XP_016861744.1:p.Pro202= | |
| NM_182760.4:c.606G>A MANE Select | NP_877437.2:p.Pro202= | |
| NM_001164674.2:c.531G>A | NP_001158146.1:p.Pro177= | |
| NM_001164675.2:c.606G>A | NP_001158147.1:p.Pro202= |