Linked Data
ClinVar Variation Id:
478247
dbSNP Id:
rs372066850
gnomAD v2:
19-38983194-G-A
gnomAD v4:
19-38492554-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38492554G>A , CM000681.2:g.38492554G>A | GRCh38 |
| NC_000019.9:g.38983194G>A , CM000681.1:g.38983194G>A | GRCh37 |
| NC_000019.8:g.43675034G>A | NCBI36 |
| NG_008866.1:g.63855G>A , LRG_766:g.63855G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.6192G>A | ENSP00000471601.2:p.Met2064Ile | |
| ENST00000359596.8:c.6192G>A MANE Select | ENSP00000352608.2:p.Met2064Ile | |
| ENST00000355481.8:c.6192G>A | ENSP00000347667.3:p.Met2064Ile | |
| ENST00000359596.7:c.6192G>A | ENSP00000352608.2:p.Met2064Ile | |
| ENST00000360985.7:c.6189G>A | ENSP00000354254.4:p.Met2063Ile | |
| NM_000540.2:c.6192G>A , LRG_766t1:c.6192G>A | NP_000531.2:p.Met2064Ile | |
| NM_001042723.1:c.6192G>A | NP_001036188.1:p.Met2064Ile | |
| XM_006723317.1:c.6192G>A | XP_006723380.1:p.Met2064Ile | |
| XM_006723319.1:c.6192G>A | XP_006723382.1:p.Met2064Ile | |
| XM_011527204.1:c.6189G>A | XP_011525506.1:p.Met2063Ile | |
| XM_011527205.1:c.6192G>A | XP_011525507.1:p.Met2064Ile | |
| XM_006723317.2:c.6192G>A | XP_006723380.1:p.Met2064Ile | |
| XM_006723319.2:c.6192G>A | XP_006723382.1:p.Met2064Ile | |
| XM_011527205.2:c.6192G>A | XP_011525507.1:p.Met2064Ile | |
| XR_001753735.1:n.6275G>A | ||
| NM_000540.3:c.6192G>A MANE Select | NP_000531.2:p.Met2064Ile | |
| NM_001042723.2:c.6192G>A | NP_001036188.1:p.Met2064Ile |