Linked Data
ClinVar Variation Id:
2010702
ClinVar RCV Id:
RCV002834187
MyVariant Identifiers:
chr14:g.91739269G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272925G>A , CM000676.2:g.91272925G>A | GRCh38 |
| NC_000014.8:g.91739269G>A , CM000676.1:g.91739269G>A | GRCh37 |
| NC_000014.7:g.90809022G>A | NCBI36 |
| NG_033118.1:g.149920C>T | |
| NG_033118.2:g.149920C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.5787C>T MANE Select | ENSP00000374507.6:p.Phe1929= | |
| ENST00000331194.8:c.1221C>T | ENSP00000330332.8:p.Phe407= | |
| ENST00000389857.10:c.5787C>T | ENSP00000374507.6:p.Phe1929= | |
| ENST00000556726.5:c.2015C>T | ||
| NM_001080414.3:c.5787C>T | NP_001073883.2:p.Phe1929= | |
| XM_011536796.1:c.5679C>T | XP_011535098.1:p.Phe1893= | |
| XM_011536796.2:c.5679C>T | XP_011535098.1:p.Phe1893= | |
| XM_017021336.1:c.2868C>T | XP_016876825.1:p.Phe956= | |
| NM_001080414.4:c.5787C>T MANE Select | NP_001073883.2:p.Phe1929= |