Linked Data
ClinVar Variation Id:
1115431
ClinVar RCV Id:
RCV001443425
dbSNP Id:
rs758811460
ExAC:
5:151202483 A / G
gnomAD v3:
5-151822922-A-G
gnomAD v4:
5-151822922-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.151822922A>G , CM000667.2:g.151822922A>G | GRCh38 |
| NC_000005.9:g.151202483A>G , CM000667.1:g.151202483A>G | GRCh37 |
| NC_000005.8:g.151182676A>G | NCBI36 |
| NG_011764.1:g.106915T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274576.9:c.1101T>C MANE Select | ENSP00000274576.5:p.Tyr367= | |
| ENST00000274576.8:c.1101T>C | ENSP00000274576.4:p.Tyr367= | |
| ENST00000455880.2:c.1125T>C | ENSP00000411593.2:p.Tyr375= | |
| ENST00000462581.6:c.*859T>C | ENSP00000430595.1:n.*859T>C | |
| NM_000171.3:c.1101T>C | NP_000162.2:p.Tyr367= | |
| NM_001146040.1:c.1125T>C | NP_001139512.1:p.Tyr375= | |
| NM_001292000.1:c.852T>C | NP_001278929.1:p.Tyr284= | |
| NM_000171.4:c.1101T>C MANE Select | NP_000162.2:p.Tyr367= | |
| NM_001146040.2:c.1125T>C | NP_001139512.1:p.Tyr375= | |
| NM_001292000.2:c.852T>C | NP_001278929.1:p.Tyr284= |