Linked Data
MyVariant Identifiers:
chr16:g.30748597T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30737276T>C , CM000678.2:g.30737276T>C | GRCh38 |
| NC_000016.9:g.30748597T>C , CM000678.1:g.30748597T>C | GRCh37 |
| NC_000016.8:g.30656098T>C | NCBI36 |
| NG_032135.1:g.43136T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000411466.7:c.7236T>C | ENSP00000405186.3:p.Thr2412= | |
| ENST00000704023.1:c.1516T>C | ||
| ENST00000706321.1:c.7236T>C | ENSP00000516346.1:p.Thr2412= | |
| ENST00000262518.9:c.7236T>C MANE Select | ENSP00000262518.4:p.Thr2412= | |
| ENST00000262518.8:c.7236T>C | ENSP00000262518.4:p.Thr2412= | |
| ENST00000380361.7:c.6705T>C | ENSP00000369719.3:p.Thr2235= | |
| ENST00000395059.6:c.6459T>C | ENSP00000378499.3:p.Thr2153= | |
| NM_006662.2:c.7236T>C | NP_006653.2:p.Thr2412= | |
| NM_006662.3:c.7236T>C MANE Select | NP_006653.2:p.Thr2412= |