Linked Data
dbSNP Id:
rs1048242618
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1986057G>C , CM000678.2:g.1986057G>C | GRCh38 |
| NC_000016.9:g.2036058G>C , CM000678.1:g.2036058G>C | GRCh37 |
| NC_000016.8:g.1976059G>C | NCBI36 |
| NG_016288.1:g.6909G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.*29G>C | ENSP00000455885.1:n.*29G>C | |
| ENST00000248114.7:c.*29G>C MANE Select | ENSP00000248114.6:n.*29G>C | |
| ENST00000248114.6:c.*29G>C | ENSP00000248114.6:n.*29G>C | |
| ENST00000565658.1:n.804G>C | ||
| ENST00000567719.1:c.*29G>C | ENSP00000455885.1:n.*29G>C | |
| ENST00000569451.1:c.*120G>C | ENSP00000456432.1:n.*120G>C | |
| NM_005262.2:c.*29G>C | NP_005253.3:n.*29G>C | |
| NM_005262.3:c.*29G>C MANE Select | NP_005253.3:n.*29G>C |