Linked Data
ClinVar Variation Id:
523738
dbSNP Id:
rs755119833
ExAC:
2:21229478 A / G
gnomAD v2:
2-21229478-A-G
gnomAD v4:
2-21006606-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21006606A>G , CM000664.2:g.21006606A>G | GRCh38 |
| NC_000002.11:g.21229478A>G , CM000664.1:g.21229478A>G | GRCh37 |
| NC_000002.10:g.21082983A>G | NCBI36 |
| NG_011793.1:g.42468T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.10262T>C MANE Select | ENSP00000233242.1:p.Met3421Thr | |
| ENST00000616098.4:c.10262T>C | ENSP00000477990.1:p.Met3421Thr | |
| NM_000384.2:c.10262T>C | NP_000375.2:p.Met3421Thr | |
| XM_011532809.1:c.5869+4127T>C | XP_011531111.1:n.5869+4127T>C | |
| NM_000384.3:c.10262T>C MANE Select | NP_000375.3:p.Met3421Thr |