Linked Data
MyVariant Identifiers:
chr16:g.223001G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173002G>C , CM000678.2:g.173002G>C | GRCh38 |
| NC_000016.9:g.223001G>C , CM000678.1:g.223001G>C | GRCh37 |
| NC_000016.8:g.163001G>C | NCBI36 |
| NG_000006.1:g.33865G>C | |
| NG_059186.1:g.1352G>C | |
| NG_059271.1:g.5156G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.90G>C MANE Select | ENSP00000251595.6:p.Leu30= | |
| ENST00000251595.10:c.90G>C | ENSP00000251595.6:p.Leu30= | |
| ENST00000397806.1:c.-2+44G>C | ENSP00000380908.1:n.-2+44G>C | |
| ENST00000482565.1:n.109G>C | ||
| ENST00000484216.1:n.59G>C | ||
| NM_000517.4:c.90G>C | NP_000508.1:p.Leu30= | |
| NM_000517.6:c.90G>C MANE Select | NP_000508.1:p.Leu30= |