Linked Data
ClinVar Variation Id:
1657647
ClinVar RCV Id:
RCV002164433
dbSNP Id:
rs748485620
ExAC:
3:119133182 C / T
gnomAD v2:
3-119133182-C-T
gnomAD v4:
3-119414335-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119414335C>T , CM000665.2:g.119414335C>T | GRCh38 |
| NC_000003.11:g.119133182C>T , CM000665.1:g.119133182C>T | GRCh37 |
| NC_000003.10:g.120615872C>T | NCBI36 |
| NG_007665.2:g.124963C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.2406C>T MANE Select | ENSP00000264245.4:p.Gly802= | |
| ENST00000264245.8:c.2406C>T | ENSP00000264245.4:p.Gly802= | |
| NM_020754.3:c.2406C>T | NP_065805.2:p.Gly802= | |
| XM_005247671.3:c.2313C>T | XP_005247728.1:p.Gly771= | |
| XM_006713714.2:c.2346C>T | XP_006713777.1:p.Gly782= | |
| XM_006713714.3:c.2346C>T | XP_006713777.1:p.Gly782= | |
| XM_017006955.1:c.1914C>T | XP_016862444.1:p.Gly638= | |
| NM_020754.4:c.2406C>T MANE Select | NP_065805.2:p.Gly802= |