Linked Data
ClinVar Variation Id:
349779
dbSNP Id:
rs201241555
ExAC:
4:79417985 C / T
gnomAD v2:
4-79417985-C-T
gnomAD v3:
4-78496831-C-T
gnomAD v4:
4-78496831-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.78496831C>T , CM000666.2:g.78496831C>T | GRCh38 |
| NC_000004.11:g.79417985C>T , CM000666.1:g.79417985C>T | GRCh37 |
| NC_000004.10:g.79637009C>T | NCBI36 |
| NG_015812.1:g.444262C>T | |
| NG_015812.2:g.444262C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682513.1:c.8985C>T | ENSP00000508201.1:p.His2995= | |
| ENST00000512123.4:c.8985C>T MANE Select | ENSP00000422834.2:p.His2995= | |
| ENST00000512123.3:c.8985C>T | ENSP00000422834.2:p.His2995= | |
| NM_025074.6:c.8985C>T | NP_079350.5:p.His2995= | |
| XM_006714314.1:c.8979C>T | XP_006714377.1:p.His2993= | |
| XM_006714316.1:c.8757C>T | XP_006714379.1:p.His2919= | |
| XM_011532270.1:c.6684C>T | XP_011530572.1:p.His2228= | |
| XM_011532271.1:c.3873C>T | XP_011530573.1:p.His1291= | |
| XM_006714316.3:c.8757C>T | XP_006714379.1:p.His2919= | |
| NM_025074.7:c.8985C>T MANE Select | NP_079350.5:p.His2995= |