Linked Data
ClinVar Variation Id:
410937
dbSNP Id:
rs1060503085
gnomAD v2:
13-48881426-G-C
gnomAD v3:
13-48307290-G-C
gnomAD v4:
13-48307290-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48307290G>C , CM000675.2:g.48307290G>C | GRCh38 |
| NC_000013.10:g.48881426G>C , CM000675.1:g.48881426G>C | GRCh37 |
| NC_000013.9:g.47779427G>C | NCBI36 |
| NG_009009.1:g.8544G>C , LRG_517:g.8544G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.148G>C MANE Select | ENSP00000267163.4:p.Glu50Gln | |
| ENST00000646097.1:c.148G>C | ENSP00000496556.1:p.Glu50Gln | |
| ENST00000650461.1:c.148G>C | ENSP00000497193.1:p.Glu50Gln | |
| ENST00000267163.4:c.148G>C | ENSP00000267163.4:p.Glu50Gln | |
| ENST00000467505.5:c.137+3241G>C | ENSP00000434702.1:n.137+3241G>C | |
| ENST00000525036.1:n.310G>C | ||
| NM_000321.2:c.148G>C , LRG_517t1:c.148G>C | NP_000312.2:p.Glu50Gln | |
| NM_000321.3:c.148G>C MANE Select | NP_000312.2:p.Glu50Gln |