Linked Data
ClinVar Variation Id:
1437120
ClinVar RCV Id:
RCV001946535
dbSNP Id:
rs139224826
ExAC:
14:74726379 G / T
gnomAD v2:
14-74726379-G-T
gnomAD v3:
14-74259676-G-T
gnomAD v4:
14-74259676-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74259676G>T , CM000676.2:g.74259676G>T | GRCh38 |
| NC_000014.8:g.74726379G>T , CM000676.1:g.74726379G>T | GRCh37 |
| NC_000014.7:g.73796132G>T | NCBI36 |
| NG_013092.1:g.25205G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261980.3:c.654G>T MANE Select | ENSP00000261980.2:p.Glu218Asp | |
| ENST00000261980.2:c.654G>T | ENSP00000261980.2:p.Glu218Asp | |
| NM_182894.2:c.654G>T | NP_878314.1:p.Glu218Asp | |
| XM_011536719.1:c.654G>T | XP_011535021.1:p.Glu218Asp | |
| NM_182894.3:c.654G>T MANE Select | NP_878314.1:p.Glu218Asp |