Linked Data
ClinVar Variation Id:
45453
ClinVar RCV Id:
RCV000404342
RCV000300529
RCV000515097
RCV000664095
RCV002464005
RCV002496613
RCV000038657
dbSNP Id:
rs141328044
ExAC:
4:6303857 G / A
gnomAD v2:
4-6303857-G-A
gnomAD v3:
4-6302130-G-A
gnomAD v4:
4-6302130-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6302130G>A , CM000666.2:g.6302130G>A | GRCh38 |
| NC_000004.11:g.6303857G>A , CM000666.1:g.6303857G>A | GRCh37 |
| NC_000004.10:g.6354758G>A | NCBI36 |
| NG_011700.1:g.37281G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682275.1:c.2371G>A | ENSP00000507852.1:p.Val791Met | |
| ENST00000683395.1:c.2312G>A | ||
| ENST00000684087.1:c.2335G>A | ENSP00000506978.1:p.Val779Met | |
| ENST00000506362.2:c.2086G>A | ENSP00000424103.2:p.Val696Met | |
| ENST00000673642.1:c.1994G>A | ENSP00000501242.1:n.1994G>A | |
| ENST00000673991.1:c.2371G>A | ENSP00000501033.1:p.Val791Met | |
| ENST00000226760.5:c.2335G>A MANE Select | ENSP00000226760.1:p.Val779Met | |
| ENST00000503569.5:c.2335G>A | ENSP00000423337.1:p.Val779Met | |
| ENST00000507765.1:n.2520G>A | ||
| NM_001145853.1:c.2335G>A | NP_001139325.1:p.Val779Met | |
| NM_006005.3:c.2335G>A MANE Select | NP_005996.2:p.Val779Met | |
| XM_017008586.1:c.2344G>A | XP_016864075.1:p.Val782Met |