Linked Data
ClinVar Variation Id:
2878662
ClinVar RCV Id:
RCV003707800
dbSNP Id:
rs192883042
ExAC:
3:142281281 C / T
gnomAD v2:
3-142281281-C-T
gnomAD v4:
3-142562439-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.142562439C>T , CM000665.2:g.142562439C>T | GRCh38 |
| NC_000003.11:g.142281281C>T , CM000665.1:g.142281281C>T | GRCh37 |
| NC_000003.10:g.143763971C>T | NCBI36 |
| NG_008951.1:g.21388G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000350721.9:c.963G>A MANE Select | ENSP00000343741.4:p.Leu321= | |
| ENST00000515149.3:c.293-1018G>A | ENSP00000425897.3:n.293-1018G>A | |
| ENST00000653868.1:n.992G>A | ||
| ENST00000657914.1:n.3321G>A | ||
| ENST00000659195.1:n.3028G>A | ||
| ENST00000661310.1:c.963G>A | ENSP00000499589.1:p.Leu321= | |
| ENST00000350721.8:c.963G>A | ENSP00000343741.4:p.Leu321= | |
| ENST00000507148.1:c.293-91G>A | ENSP00000426595.1:n.293-91G>A | |
| ENST00000515149.2:c.6G>A | ENSP00000425897.2:p.Leu2= | |
| NM_001184.3:c.963G>A | NP_001175.2:p.Leu321= | |
| XM_011512924.1:c.963G>A | XP_011511226.1:p.Leu321= | |
| XM_011512925.1:c.963G>A | XP_011511227.1:p.Leu321= | |
| XM_011512926.1:c.963G>A | XP_011511228.1:p.Leu321= | |
| XM_011512927.1:c.963G>A | XP_011511229.1:p.Leu321= | |
| XR_924147.1:n.1052G>A | ||
| XR_924148.1:n.1052G>A | ||
| XR_924149.1:n.1052G>A | ||
| NM_001354579.1:c.963G>A | NP_001341508.1:p.Leu321= | |
| XR_001740179.2:n.1052G>A | ||
| XR_001740180.2:n.1052G>A | ||
| XR_001740181.2:n.1052G>A | ||
| XR_001740182.1:n.1052G>A | ||
| XR_002959543.1:n.1052G>A | ||
| XR_924148.2:n.1052G>A | ||
| NM_001184.4:c.963G>A MANE Select | NP_001175.2:p.Leu321= | |
| NM_001354579.2:c.963G>A | NP_001341508.1:p.Leu321= |