Linked Data
ClinVar Variation Id:
92895
ClinVar RCV Id:
RCV000078701
RCV000671886
RCV001150122
RCV001150123
RCV001511461
RCV001573681
RCV004542751
dbSNP Id:
rs34421970
ExAC:
3:33059981 G / A
gnomAD v2:
3-33059981-G-A
gnomAD v3:
3-33018489-G-A
gnomAD v4:
3-33018489-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.33018489G>A , CM000665.2:g.33018489G>A | GRCh38 |
| NC_000003.11:g.33059981G>A , CM000665.1:g.33059981G>A | GRCh37 |
| NC_000003.10:g.33034985G>A | NCBI36 |
| NG_009005.1:g.83714C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307363.10:c.1306C>T MANE Select | ENSP00000306920.4:p.Leu436Phe | |
| ENST00000307363.9:c.1306C>T | ENSP00000306920.4:p.Leu436Phe | |
| ENST00000307377.12:c.913C>T | ENSP00000305920.8:p.Leu305Phe | |
| ENST00000399402.7:c.1216C>T | ENSP00000382333.2:p.Leu406Phe | |
| ENST00000461475.5:n.405C>T | ||
| ENST00000467571.5:n.343C>T | ||
| ENST00000497796.5:n.558C>T | ||
| NM_000404.2:c.1306C>T | NP_000395.2:p.Leu436Phe | |
| NM_000404.3:c.1306C>T | NP_000395.2:p.Leu436Phe | |
| NM_001079811.1:c.1216C>T | NP_001073279.1:p.Leu406Phe | |
| NM_001079811.2:c.1216C>T | NP_001073279.1:p.Leu406Phe | |
| NM_001135602.1:c.913C>T | NP_001129074.1:p.Leu305Phe | |
| NM_001135602.2:c.913C>T | NP_001129074.1:p.Leu305Phe | |
| NM_001317040.1:c.1450C>T | NP_001303969.1:p.Leu484Phe | |
| NM_000404.4:c.1306C>T MANE Select | NP_000395.3:p.Leu436Phe | |
| NM_001079811.3:c.1216C>T | NP_001073279.2:p.Leu406Phe | |
| NM_001135602.3:c.913C>T | NP_001129074.2:p.Leu305Phe | |
| NM_001317040.2:c.1450C>T | NP_001303969.2:p.Leu484Phe | |
| NM_001393580.1:c.1306C>T | NP_001380509.1:p.Leu436Phe |