Linked Data
MyVariant Identifiers:
chr16:g.223578G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173579G>C , CM000678.2:g.173579G>C | GRCh38 |
| NC_000016.9:g.223578G>C , CM000678.1:g.223578G>C | GRCh37 |
| NC_000016.8:g.163578G>C | NCBI36 |
| NG_000006.1:g.34442G>C | |
| NG_059186.1:g.1929G>C | |
| NG_059271.1:g.5733G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.408G>C MANE Select | ENSP00000251595.6:p.Val136= | |
| ENST00000251595.10:c.408G>C | ENSP00000251595.6:p.Val136= | |
| ENST00000397806.1:c.312G>C | ENSP00000380908.1:p.Val104= | |
| ENST00000482565.1:n.544G>C | ||
| NM_000517.4:c.408G>C | NP_000508.1:p.Val136= | |
| NM_000517.6:c.408G>C MANE Select | NP_000508.1:p.Val136= |