Linked Data
ClinVar Variation Id:
2032405
ClinVar RCV Id:
RCV002884944
gnomAD v4:
14-28768536-C-T
MyVariant Identifiers:
chr14:g.29237742C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28768536C>T , CM000676.2:g.28768536C>T | GRCh38 |
| NC_000014.8:g.29237742C>T , CM000676.1:g.29237742C>T | GRCh37 |
| NC_000014.7:g.28307493C>T | NCBI36 |
| NG_009367.1:g.6456C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706482.1:c.1257C>T | ENSP00000516406.1:p.Pro419= | |
| ENST00000313071.7:c.1257C>T MANE Select | ENSP00000339004.3:p.Pro419= | |
| ENST00000313071.6:c.1257C>T | ENSP00000339004.3:p.Pro419= | |
| NM_005249.4:c.1257C>T | NP_005240.3:p.Pro419= | |
| NM_005249.5:c.1257C>T MANE Select | NP_005240.3:p.Pro419= |