Linked Data
ClinVar Variation Id:
756833
dbSNP Id:
rs1019544911
gnomAD v2:
11-47355274-G-T
gnomAD v3:
11-47333723-G-T
gnomAD v4:
11-47333723-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47333723G>T , CM000673.2:g.47333723G>T | GRCh38 |
| NC_000011.9:g.47355274G>T , CM000673.1:g.47355274G>T | GRCh37 |
| NC_000011.8:g.47311850G>T | NCBI36 |
| NG_007667.1:g.23980C>A , LRG_386:g.23980C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545968.6:c.3024C>A MANE Select | ENSP00000442795.1:p.Thr1008= | |
| ENST00000256993.8:c.3024C>A | ENSP00000256993.5:p.Thr1008= | |
| ENST00000399249.6:c.3024C>A | ENSP00000382193.2:p.Thr1008= | |
| ENST00000545968.5:c.3024C>A | ENSP00000442795.1:p.Thr1008= | |
| NM_000256.3:c.3024C>A , LRG_386t1:c.3024C>A MANE Select | NP_000247.2:p.Thr1008= | |
| XM_011520117.1:c.3006C>A | XP_011518419.1:p.Thr1002= | |
| XM_011520118.1:c.2943C>A | XP_011518420.1:p.Thr981= |