Linked Data
ClinVar Variation Id:
572128
ClinVar RCV Id:
RCV000693443
dbSNP Id:
rs1201977804
gnomAD v4:
13-48304010-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48304010C>T , CM000675.2:g.48304010C>T | GRCh38 |
| NC_000013.10:g.48878146C>T , CM000675.1:g.48878146C>T | GRCh37 |
| NC_000013.9:g.47776147C>T | NCBI36 |
| NG_009009.1:g.5264C>T , LRG_517:g.5264C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.98C>T MANE Select | ENSP00000267163.4:p.Pro33Leu | |
| ENST00000646097.1:c.98C>T | ENSP00000496556.1:p.Pro33Leu | |
| ENST00000650461.1:c.98C>T | ENSP00000497193.1:p.Pro33Leu | |
| ENST00000267163.4:c.98C>T | ENSP00000267163.4:p.Pro33Leu | |
| ENST00000467505.5:c.98C>T | ENSP00000434702.1:p.Pro33Leu | |
| ENST00000525036.1:n.260C>T | ||
| NM_000321.2:c.98C>T , LRG_517t1:c.98C>T | NP_000312.2:p.Pro33Leu | |
| NM_000321.3:c.98C>T MANE Select | NP_000312.2:p.Pro33Leu |