Linked Data
ClinVar Variation Id:
285832
dbSNP Id:
rs886043228
gnomAD v3:
4-52029762-G-A
gnomAD v4:
4-52029762-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52029762G>A , CM000666.2:g.52029762G>A | GRCh38 |
| NC_000004.11:g.52895928G>A , CM000666.1:g.52895928G>A | GRCh37 |
| NC_000004.10:g.52590685G>A | NCBI36 |
| NG_008891.1:g.13558C>T , LRG_204:g.13558C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.345C>T MANE Select | ENSP00000370839.6:p.Asp115= | |
| ENST00000381431.9:c.345C>T | ENSP00000370839.5:p.Asp115= | |
| ENST00000506357.5:c.428C>T | ||
| ENST00000514133.1:c.422C>T | ENSP00000425818.1:n.422C>T | |
| NM_000232.4:c.345C>T , LRG_204t1:c.345C>T | NP_000223.1:p.Asp115= | |
| XM_006714049.2:c.48C>T | XP_006714112.1:p.Asp16= | |
| XM_011534403.1:c.135C>T | XP_011532705.1:p.Asp45= | |
| XM_011534404.1:c.48C>T | XP_011532706.1:p.Asp16= | |
| NM_000232.5:c.345C>T MANE Select | NP_000223.1:p.Asp115= |