Linked Data
dbSNP Id:
rs1212970570
gnomAD v2:
11-67353999-C-T
gnomAD v3:
11-67586528-C-T
gnomAD v4:
11-67586528-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67586528C>T , CM000673.2:g.67586528C>T | GRCh38 |
| NC_000011.9:g.67353999C>T , CM000673.1:g.67353999C>T | GRCh37 |
| NC_000011.8:g.67110575C>T | NCBI36 |
| NG_012075.1:g.7934C>T , LRG_723:g.7934C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.476C>T | ENSP00000381604.1:p.Ala159Val | |
| ENST00000398606.10:c.584C>T MANE Select | ENSP00000381607.3:p.Ala195Val | |
| ENST00000398603.5:c.476C>T | ENSP00000381604.1:p.Ala159Val | |
| ENST00000398606.7:c.584C>T | ENSP00000381607.3:p.Ala195Val | |
| ENST00000467591.1:n.695C>T | ||
| ENST00000494593.1:n.1556C>T | ||
| ENST00000498765.5:c.647C>T | ||
| NM_000852.3:c.584C>T , LRG_723t1:c.584C>T | NP_000843.1:p.Ala195Val | |
| NM_000852.4:c.584C>T MANE Select | NP_000843.1:p.Ala195Val |