Linked Data
dbSNP Id:
rs2150889824
gnomAD v4:
6-35455765-A-G
MyVariant Identifiers:
chr6:g.35423542A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35455765A>G , CM000668.2:g.35455765A>G | GRCh38 |
| NC_000006.11:g.35423542A>G , CM000668.1:g.35423542A>G | GRCh37 |
| NC_000006.10:g.35531520A>G | NCBI36 |
| NG_011708.1:g.8405A>G , LRG_498:g.8405A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696264.1:c.267A>G | ENSP00000512511.1:p.Arg89= | |
| ENST00000696265.1:c.267A>G | ENSP00000512512.1:p.Arg89= | |
| ENST00000229769.3:c.267A>G MANE Select | ENSP00000229769.2:p.Arg89= | |
| ENST00000648059.1:c.267A>G | ENSP00000497902.1:p.Arg89= | |
| ENST00000229769.2:c.267A>G | ENSP00000229769.2:p.Arg89= | |
| NM_021922.2:c.267A>G , LRG_498t1:c.267A>G | NP_068741.1:p.Arg89= | |
| XM_005248885.2:c.267A>G | XP_005248942.1:p.Arg89= | |
| XM_005248886.2:c.267A>G | XP_005248943.1:p.Arg89= | |
| XM_005248887.2:c.267A>G | XP_005248944.1:p.Arg89= | |
| XM_005248888.2:c.267A>G | XP_005248945.1:p.Arg89= | |
| XM_011514343.1:c.-28A>G | XP_011512645.1:n.-28A>G | |
| XM_011514344.1:c.-28A>G | XP_011512646.1:n.-28A>G | |
| XM_005248888.3:c.267A>G | XP_005248945.1:p.Arg89= | |
| XM_011514343.2:c.-28A>G | XP_011512645.1:n.-28A>G | |
| XR_001743226.1:n.474A>G | ||
| XR_002956267.1:n.474A>G | ||
| NM_021922.3:c.267A>G MANE Select | NP_068741.1:p.Arg89= |