Linked Data
MyVariant Identifiers:
chr16:g.88786138A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88719730A>C , CM000678.2:g.88719730A>C | GRCh38 |
| NC_000016.9:g.88786138A>C , CM000678.1:g.88786138A>C | GRCh37 |
| NC_000016.8:g.87313639A>C | NCBI36 |
| NG_042229.1:g.70491T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301015.14:c.6324-9T>G MANE Select | ENSP00000301015.9:n.6324-9T>G | |
| ENST00000466823.3:c.350-9T>G | ||
| ENST00000301015.13:c.6324-9T>G | ENSP00000301015.9:n.6324-9T>G | |
| ENST00000419505.5:c.90-9T>G | ENSP00000406358.1:n.90-9T>G | |
| ENST00000466823.2:c.350-9T>G | ||
| ENST00000495568.7:n.565-9T>G | ||
| ENST00000497793.2:n.479-9T>G | ||
| NM_001142864.2:c.6324-9T>G | NP_001136336.2:n.6324-9T>G | |
| NM_001142864.3:c.6324-9T>G | NP_001136336.2:n.6324-9T>G | |
| NM_001142864.4:c.6324-9T>G MANE Select | NP_001136336.2:n.6324-9T>G |