Linked Data
MyVariant Identifiers:
chr16:g.67470002G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67436099G>T , CM000678.2:g.67436099G>T | GRCh38 |
| NC_000016.9:g.67470002G>T , CM000678.1:g.67470002G>T | GRCh37 |
| NC_000016.8:g.66027503G>T | NCBI36 |
| NG_011482.1:g.50088C>A | |
| NG_016549.1:g.9967G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326152.6:c.621G>T MANE Select | ENSP00000316786.5:p.Leu207= | |
| ENST00000326152.5:c.621G>T | ENSP00000316786.5:p.Leu207= | |
| ENST00000566606.1:c.599G>T | ENSP00000473429.1:n.599G>T | |
| ENST00000567684.2:n.484G>T | ||
| NM_000196.3:c.621G>T | NP_000187.3:p.Leu207= | |
| NM_000196.4:c.621G>T MANE Select | NP_000187.3:p.Leu207= |