Linked Data
dbSNP Id:
rs1598202334
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67940004T>G , CM000678.2:g.67940004T>G | GRCh38 |
| NC_000016.9:g.67973907T>G , CM000678.1:g.67973907T>G | GRCh37 |
| NC_000016.8:g.66531408T>G | NCBI36 |
| NG_009778.1:g.9109A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.1223A>C MANE Select | ENSP00000264005.5:p.Asn408Thr | |
| ENST00000264005.9:c.1223A>C | ENSP00000264005.5:p.Asn408Thr | |
| ENST00000570369.5:c.226A>C | ||
| ENST00000573538.5:c.961A>C | ENSP00000463220.1:n.961A>C | |
| NM_000229.1:c.1223A>C | NP_000220.1:p.Asn408Thr | |
| NM_000229.2:c.1223A>C MANE Select | NP_000220.1:p.Asn408Thr |