Linked Data
ClinVar Variation Id:
849728
ClinVar RCV Id:
RCV001053753
dbSNP Id:
rs899277811
gnomAD v2:
2-38302293-C-G
gnomAD v3:
2-38075150-C-G
gnomAD v4:
2-38075150-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38075150C>G , CM000664.2:g.38075150C>G | GRCh38 |
| NC_000002.11:g.38302293C>G , CM000664.1:g.38302293C>G | GRCh37 |
| NC_000002.10:g.38155797C>G | NCBI36 |
| NG_008386.2:g.5952G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000490576.2:c.239G>C | ENSP00000478839.2:p.Arg80Pro | |
| ENST00000610745.5:c.239G>C MANE Select | ENSP00000478561.1:p.Arg80Pro | |
| ENST00000490576.1:c.239G>C | ENSP00000478839.1:p.Arg80Pro | |
| ENST00000494864.1:c.-70-3840G>C | ENSP00000479876.1:n.-70-3840G>C | |
| ENST00000610745.4:c.239G>C | ENSP00000478561.1:p.Arg80Pro | |
| ENST00000613082.1:n.375+630G>C | ||
| ENST00000614273.1:c.239G>C | ENSP00000483678.1:p.Arg80Pro | |
| NM_000104.3:c.239G>C | NP_000095.2:p.Arg80Pro | |
| NM_000104.4:c.239G>C MANE Select | NP_000095.2:p.Arg80Pro |