Linked Data
dbSNP Id:
rs111033598
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173212G>C , CM000678.2:g.173212G>C | GRCh38 |
| NC_000016.9:g.223211G>C , CM000678.1:g.223211G>C | GRCh37 |
| NC_000016.8:g.163211G>C | NCBI36 |
| NG_000006.1:g.34075G>C | |
| NG_059186.1:g.1562G>C | |
| NG_059271.1:g.5366G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.183G>C MANE Select | ENSP00000251595.6:p.Lys61Asn | |
| ENST00000251595.10:c.183G>C | ENSP00000251595.6:p.Lys61Asn | |
| ENST00000397806.1:c.87G>C | ENSP00000380908.1:p.Lys29Asn | |
| ENST00000482565.1:n.319G>C | ||
| ENST00000484216.1:n.152G>C | ||
| NM_000517.4:c.183G>C | NP_000508.1:p.Lys61Asn | |
| NM_000517.6:c.183G>C MANE Select | NP_000508.1:p.Lys61Asn |