Linked Data
ClinVar Variation Id:
225407
dbSNP Id:
rs80358317
ExAC:
11:68192694 A / G
gnomAD v2:
11-68192694-A-G
gnomAD v3:
11-68425226-A-G
gnomAD v4:
11-68425226-A-G
PubMed:
PMID:15981244
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68425226A>G , CM000673.2:g.68425226A>G | GRCh38 |
| NC_000011.9:g.68192694A>G , CM000673.1:g.68192694A>G | GRCh37 |
| NC_000011.8:g.67949270A>G | NCBI36 |
| NG_015835.1:g.117587A>G | |
| NG_015835.2:g.117587A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000294304.12:c.3361A>G MANE Select | ENSP00000294304.6:p.Asn1121Asp | |
| ENST00000294304.11:c.3361A>G | ENSP00000294304.6:p.Asn1121Asp | |
| ENST00000529993.5:c.*1967A>G | ENSP00000436652.1:n.*1967A>G | |
| NM_001291902.1:c.1618A>G | NP_001278831.1:p.Asn540Asp | |
| NM_002335.3:c.3361A>G | NP_002326.2:p.Asn1121Asp | |
| XM_005273994.2:c.3361A>G | XP_005274051.1:p.Asn1121Asp | |
| XM_011545029.1:c.3388A>G | XP_011543331.1:p.Asn1130Asp | |
| XM_011545030.1:c.3388A>G | XP_011543332.1:p.Asn1130Asp | |
| XM_011545031.1:c.3388A>G | XP_011543333.1:p.Asn1130Asp | |
| XR_949925.1:n.3403A>G | ||
| XR_949926.1:n.3403A>G | ||
| XM_017017735.1:c.1618A>G | XP_016873224.1:p.Asn540Asp | |
| XM_017017736.1:c.901A>G | XP_016873225.1:p.Asn301Asp | |
| XR_949925.2:n.3403A>G | ||
| XR_949926.2:n.3403A>G | ||
| NM_002335.4:c.3361A>G MANE Select | NP_002326.2:p.Asn1121Asp | |
| NM_001291902.2:c.1618A>G | NP_001278831.1:p.Asn540Asp |