Linked Data
ClinVar Variation Id:
431884
dbSNP Id:
rs140526335
ExAC:
9:2639898 A / G
gnomAD v2:
9-2639898-A-G
gnomAD v3:
9-2639898-A-G
gnomAD v4:
9-2639898-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.2639898A>G , CM000671.2:g.2639898A>G | GRCh38 |
| NC_000009.11:g.2639898A>G , CM000671.1:g.2639898A>G | GRCh37 |
| NC_000009.10:g.2629898A>G | NCBI36 |
| NG_012741.1:g.23106A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000382096.6:c.242A>G | ENSP00000371528.2:p.Asn81Ser | |
| ENST00000382100.8:c.242A>G MANE Select | ENSP00000371532.2:p.Asn81Ser | |
| ENST00000679851.1:n.227A>G | ||
| ENST00000680021.1:n.442A>G | ||
| ENST00000680243.1:c.*21A>G | ENSP00000505911.1:n.*21A>G | |
| ENST00000680746.1:c.242A>G | ENSP00000505030.1:p.Asn81Ser | |
| ENST00000680891.1:c.*37A>G | ENSP00000505167.1:n.*37A>G | |
| ENST00000681306.1:c.242A>G | ENSP00000506072.1:p.Asn81Ser | |
| ENST00000681618.1:c.242A>G | ENSP00000505773.1:p.Asn81Ser | |
| ENST00000681644.1:c.*37A>G | ENSP00000505180.1:n.*37A>G | |
| ENST00000681770.1:n.230A>G | ||
| ENST00000681806.1:c.242A>G | ENSP00000505282.1:p.Asn81Ser | |
| ENST00000382096.5:c.242A>G | ENSP00000371528.1:p.Asn81Ser | |
| ENST00000382099.2:c.242A>G | ENSP00000371531.2:p.Asn81Ser | |
| ENST00000382100.7:c.242A>G | ENSP00000371532.2:p.Asn81Ser | |
| NM_001018056.1:c.242A>G | NP_001018066.1:p.Asn81Ser | |
| NM_003383.3:c.242A>G | NP_003374.3:p.Asn81Ser | |
| XM_011518029.1:c.242A>G | XP_011516331.1:p.Asn81Ser | |
| NM_001018056.2:c.242A>G | NP_001018066.1:p.Asn81Ser | |
| NM_001322225.1:c.242A>G | NP_001309154.1:p.Asn81Ser | |
| NM_001322226.1:c.242A>G | NP_001309155.1:p.Asn81Ser | |
| NM_003383.4:c.242A>G | NP_003374.3:p.Asn81Ser | |
| XR_001746373.2:n.646A>G | ||
| XR_002956805.1:n.646A>G | ||
| NM_003383.5:c.242A>G MANE Select | NP_003374.3:p.Asn81Ser | |
| NM_001018056.3:c.242A>G | NP_001018066.1:p.Asn81Ser | |
| NM_001322225.2:c.242A>G | NP_001309154.1:p.Asn81Ser | |
| NM_001322226.2:c.242A>G | NP_001309155.1:p.Asn81Ser |