Linked Data
dbSNP Id:
rs1344128007
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10152566C>G , CM000665.2:g.10152566C>G | GRCh38 |
| NC_000003.11:g.10194250C>G , CM000665.1:g.10194250C>G | GRCh37 |
| NC_000003.10:g.10169250C>G | NCBI36 |
| NG_008212.3:g.15932C>G , LRG_322:g.15932C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696153.1:c.*2601C>G | ENSP00000512444.1:n.*2601C>G | |
| ENST00000256474.3:c.*2601C>G MANE Select | ENSP00000256474.3:n.*2601C>G | |
| NM_000551.3:c.*2601C>G , LRG_322t1:c.*2601C>G | NP_000542.1:n.*2601C>G | |
| NM_198156.2:c.*2601C>G | NP_937799.1:n.*2601C>G | |
| NM_001354723.1:c.*2797C>G | NP_001341652.1:n.*2797C>G | |
| NM_000551.4:c.*2601C>G MANE Select | NP_000542.1:n.*2601C>G | |
| NM_001354723.2:c.*2797C>G | NP_001341652.1:n.*2797C>G | |
| NM_198156.3:c.*2601C>G | NP_937799.1:n.*2601C>G |