Linked Data
ClinVar Variation Id:
314622
ClinVar RCV Id:
RCV000308277
dbSNP Id:
rs10147023
gnomAD v2:
14-77975925-C-T
gnomAD v3:
14-77509582-C-T
gnomAD v4:
14-77509582-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.77509582C>T , CM000676.2:g.77509582C>T | GRCh38 |
| NC_000014.8:g.77975925C>T , CM000676.1:g.77975925C>T | GRCh37 |
| NC_000014.7:g.77045678C>T | NCBI36 |
| NG_028282.1:g.112186G>A , LRG_371:g.112186G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686627.1:n.3423G>A | ||
| ENST00000687688.1:n.4154G>A | ||
| ENST00000692906.1:n.4123G>A | ||
| ENST00000216484.7:c.*2702G>A MANE Select | ENSP00000216484.2:n.*2702G>A | |
| ENST00000216484.6:c.*2702G>A | ENSP00000216484.2:n.*2702G>A | |
| NM_004863.3:c.*2702G>A , LRG_371t1:c.*2702G>A | NP_004854.1:n.*2702G>A | |
| NM_004863.4:c.*2702G>A MANE Select | NP_004854.1:n.*2702G>A |