Linked Data
ClinVar Variation Id:
2947877
ClinVar RCV Id:
RCV003804507
MyVariant Identifiers:
chr5:g.149357491C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149977928C>T , CM000667.2:g.149977928C>T | GRCh38 |
| NC_000005.9:g.149357491C>T , CM000667.1:g.149357491C>T | GRCh37 |
| NC_000005.8:g.149337684C>T | NCBI36 |
| NG_007147.2:g.19046C>T , LRG_684:g.19046C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000690410.1:n.508C>T | ||
| ENST00000286298.5:c.276C>T MANE Select | ENSP00000286298.4:p.Phe92= | |
| ENST00000286298.4:c.276C>T | ENSP00000286298.4:p.Phe92= | |
| NM_000112.3:c.276C>T , LRG_684t1:c.276C>T | NP_000103.2:p.Phe92= | |
| XM_017009191.2:c.276C>T | XP_016864680.1:p.Phe92= | |
| NM_000112.4:c.276C>T MANE Select | NP_000103.2:p.Phe92= |