Linked Data
ClinVar Variation Id:
2317387
ClinVar RCV Id:
RCV004159634
dbSNP Id:
rs776223203
ExAC:
3:39307151 T / C
gnomAD v2:
3-39307151-T-C
gnomAD v4:
3-39265660-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.39265660T>C , CM000665.2:g.39265660T>C | GRCh38 |
| NC_000003.11:g.39307151T>C , CM000665.1:g.39307151T>C | GRCh37 |
| NC_000003.10:g.39282155T>C | NCBI36 |
| NG_016362.1:g.21076A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399220.3:c.850A>G MANE Select | ENSP00000382166.3:p.Ser284Gly | |
| ENST00000358309.3:c.946A>G | ENSP00000351059.3:p.Ser316Gly | |
| ENST00000399220.2:c.850A>G | ENSP00000382166.2:p.Ser284Gly | |
| ENST00000541347.5:c.850A>G | ENSP00000439140.1:p.Ser284Gly | |
| ENST00000542107.5:c.850A>G | ENSP00000444928.1:p.Ser284Gly | |
| NM_001171171.1:c.850A>G | NP_001164642.1:p.Ser284Gly | |
| NM_001171172.1:c.850A>G | NP_001164643.1:p.Ser284Gly | |
| NM_001171174.1:c.946A>G | NP_001164645.1:p.Ser316Gly | |
| NM_001337.3:c.850A>G | NP_001328.1:p.Ser284Gly | |
| NM_001337.4:c.850A>G MANE Select | NP_001328.1:p.Ser284Gly | |
| NM_001171171.2:c.850A>G | NP_001164642.1:p.Ser284Gly | |
| NM_001171172.2:c.850A>G | NP_001164643.1:p.Ser284Gly |