Linked Data
MyVariant Identifiers:
chr16:g.227126C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177127C>T , CM000678.2:g.177127C>T | GRCh38 |
| NC_000016.9:g.227126C>T , CM000678.1:g.227126C>T | GRCh37 |
| NC_000016.8:g.167126C>T | NCBI36 |
| NG_000006.1:g.37990C>T | |
| NG_059186.1:g.5477C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320868.9:c.294C>T MANE Select | ENSP00000322421.5:p.Asn98= | |
| ENST00000397797.1:c.198C>T | ENSP00000380899.1:p.Asn66= | |
| ENST00000472694.1:n.430C>T | ||
| ENST00000487791.1:n.263C>T | ||
| NM_000558.4:c.294C>T | NP_000549.1:p.Asn98= | |
| NM_000558.5:c.294C>T MANE Select | NP_000549.1:p.Asn98= |