Linked Data
ClinVar Variation Id:
438005
dbSNP Id:
rs1553257498
gnomAD v4:
1-215741386-G-T
PubMed:
PMID:28041643
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215741386G>T , CM000663.2:g.215741386G>T | GRCh38 |
| NC_000001.10:g.215914728G>T , CM000663.1:g.215914728G>T | GRCh37 |
| NC_000001.9:g.213981351G>T | NCBI36 |
| NG_009497.1:g.687011C>A | |
| NG_009497.2:g.687063C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.11700C>A MANE Select | ENSP00000305941.3:p.Tyr3900Ter | |
| ENST00000674083.1:c.11700C>A | ENSP00000501296.1:p.Tyr3900Ter | |
| ENST00000307340.7:c.11700C>A | ENSP00000305941.3:p.Tyr3900Ter | |
| NM_206933.2:c.11700C>A | NP_996816.2:p.Tyr3900Ter | |
| NM_206933.3:c.11700C>A | NP_996816.2:p.Tyr3900Ter | |
| NM_206933.4:c.11700C>A MANE Select | NP_996816.3:p.Tyr3900Ter |