Linked Data
ClinVar Variation Id:
1038484
ClinVar RCV Id:
RCV001341801
dbSNP Id:
rs1908199604
gnomAD v3:
17-72123966-C-T
gnomAD v4:
17-72123966-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.72123966C>T , CM000679.2:g.72123966C>T | GRCh38 |
| NC_000017.10:g.70120107C>T , CM000679.1:g.70120107C>T | GRCh37 |
| NC_000017.9:g.67631702C>T | NCBI36 |
| NG_012490.1:g.7947C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000245479.3:c.1109C>T MANE Select | ENSP00000245479.2:p.Pro370Leu | |
| ENST00000245479.2:c.1109C>T | ENSP00000245479.2:p.Pro370Leu | |
| NM_000346.3:c.1109C>T | NP_000337.1:p.Pro370Leu | |
| NM_000346.4:c.1109C>T MANE Select | NP_000337.1:p.Pro370Leu |