Linked Data
ClinVar Variation Id:
349762
dbSNP Id:
rs886059635
gnomAD v2:
4-79399121-C-T
gnomAD v3:
4-78477967-C-T
gnomAD v4:
4-78477967-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.78477967C>T , CM000666.2:g.78477967C>T | GRCh38 |
| NC_000004.11:g.79399121C>T , CM000666.1:g.79399121C>T | GRCh37 |
| NC_000004.10:g.79618145C>T | NCBI36 |
| NG_015812.1:g.425398C>T | |
| NG_015812.2:g.425398C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682513.1:c.8004C>T | ENSP00000508201.1:p.Asn2668= | |
| ENST00000512123.4:c.8004C>T MANE Select | ENSP00000422834.2:p.Asn2668= | |
| ENST00000512123.3:c.8004C>T | ENSP00000422834.2:p.Asn2668= | |
| NM_025074.6:c.8004C>T | NP_079350.5:p.Asn2668= | |
| XM_006714314.1:c.7998C>T | XP_006714377.1:p.Asn2666= | |
| XM_006714316.1:c.7776C>T | XP_006714379.1:p.Asn2592= | |
| XM_011532270.1:c.5703C>T | XP_011530572.1:p.Asn1901= | |
| XM_011532271.1:c.2892C>T | XP_011530573.1:p.Asn964= | |
| XM_006714316.3:c.7776C>T | XP_006714379.1:p.Asn2592= | |
| NM_025074.7:c.8004C>T MANE Select | NP_079350.5:p.Asn2668= |