Linked Data
ClinVar Variation Id:
222702
dbSNP Id:
rs869025461
gnomAD v4:
11-47333584-T-A
PubMed:
PMID:22267749
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47333584T>A , CM000673.2:g.47333584T>A | GRCh38 |
| NC_000011.9:g.47355135T>A , CM000673.1:g.47355135T>A | GRCh37 |
| NC_000011.8:g.47311711T>A | NCBI36 |
| NG_007667.1:g.24119A>T , LRG_386:g.24119A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000545968.6:c.3163A>T MANE Select | ENSP00000442795.1:p.Lys1055Ter | |
| ENST00000256993.8:c.3163A>T | ENSP00000256993.5:p.Lys1055Ter | |
| ENST00000399249.6:c.3163A>T | ENSP00000382193.2:p.Lys1055Ter | |
| ENST00000545968.5:c.3163A>T | ENSP00000442795.1:p.Lys1055Ter | |
| NM_000256.3:c.3163A>T , LRG_386t1:c.3163A>T MANE Select | NP_000247.2:p.Lys1055Ter | |
| XM_011520117.1:c.3145A>T | XP_011518419.1:p.Lys1049Ter | |
| XM_011520118.1:c.3082A>T | XP_011518420.1:p.Lys1028Ter |