Linked Data
dbSNP Id:
rs1357359928
gnomAD v3:
12-6870524-T-C
gnomAD v4:
12-6870524-T-C
MyVariant Identifiers:
chr12:g.6870524T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6870524T>C , CM000674.2:g.6870524T>C | GRCh38 |
| NC_000012.11:g.6979688T>C , CM000674.1:g.6979688T>C | GRCh37 |
| NC_000012.10:g.6849949T>C | NCBI36 |
| NG_011948.1:g.8105T>C | |
| NG_013308.1:g.7834A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396705.10:c.*141T>C MANE Select | ENSP00000379933.4:n.*141T>C | |
| ENST00000229270.8:c.*141T>C | ENSP00000229270.4:n.*141T>C | |
| ENST00000396705.9:c.*141T>C | ENSP00000379933.4:n.*141T>C | |
| ENST00000474253.1:n.380T>C | ||
| ENST00000535434.5:c.*141T>C | ENSP00000443599.1:n.*141T>C | |
| ENST00000613953.4:c.*141T>C | ENSP00000484435.1:n.*141T>C | |
| NM_000365.5:c.*141T>C | NP_000356.1:n.*141T>C | |
| NM_001159287.1:c.*141T>C | NP_001152759.1:n.*141T>C | |
| NM_001258026.1:c.*141T>C | NP_001244955.1:n.*141T>C | |
| XR_002957378.1:n.1899T>C | ||
| NM_000365.6:c.*141T>C MANE Select | NP_000356.1:n.*141T>C | |
| NM_001258026.2:c.*141T>C | NP_001244955.1:n.*141T>C |