Linked Data
ClinVar Variation Id:
1743946
dbSNP Id:
rs2138027367
gnomAD v4:
13-48303960-C-T
MyVariant Identifiers:
chr13:g.48878096C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48303960C>T , CM000675.2:g.48303960C>T | GRCh38 |
| NC_000013.10:g.48878096C>T , CM000675.1:g.48878096C>T | GRCh37 |
| NC_000013.9:g.47776097C>T | NCBI36 |
| NG_009009.1:g.5214C>T , LRG_517:g.5214C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.48C>T MANE Select | ENSP00000267163.4:p.Ala16= | |
| ENST00000646097.1:c.48C>T | ENSP00000496556.1:p.Ala16= | |
| ENST00000650461.1:c.48C>T | ENSP00000497193.1:p.Ala16= | |
| ENST00000267163.4:c.48C>T | ENSP00000267163.4:p.Ala16= | |
| ENST00000467505.5:c.48C>T | ENSP00000434702.1:p.Ala16= | |
| ENST00000525036.1:n.210C>T | ||
| NM_000321.2:c.48C>T , LRG_517t1:c.48C>T | NP_000312.2:p.Ala16= | |
| NM_000321.3:c.48C>T MANE Select | NP_000312.2:p.Ala16= |