Linked Data
dbSNP Id:
rs1450175936
gnomAD v2:
11-1075819-C-T
gnomAD v3:
11-1075819-C-T
gnomAD v4:
11-1075819-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1075819C>T , CM000673.2:g.1075819C>T | GRCh38 |
| NC_000011.9:g.1075819C>T , CM000673.1:g.1075819C>T | GRCh37 |
| NC_000011.8:g.1065819C>T | NCBI36 |
| NG_051929.1:g.5945C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361558.7:n.272C>T | ||
| ENST00000675028.1:c.245C>T | ENSP00000502432.1:p.Pro82Leu | |
| NM_002457.3:c.245C>T | NP_002448.3:p.Pro82Leu | |
| NM_002457.4:c.245C>T | NP_002448.4:p.Pro82Leu |