Linked Data
MyVariant Identifiers:
chr16:g.88786203C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88719795C>T , CM000678.2:g.88719795C>T | GRCh38 |
| NC_000016.9:g.88786203C>T , CM000678.1:g.88786203C>T | GRCh37 |
| NC_000016.8:g.87313704C>T | NCBI36 |
| NG_042229.1:g.70426G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301015.14:c.6323+7G>A MANE Select | ENSP00000301015.9:n.6323+7G>A | |
| ENST00000466823.3:c.349+7G>A | ||
| ENST00000301015.13:c.6323+7G>A | ENSP00000301015.9:n.6323+7G>A | |
| ENST00000419505.5:c.89+7G>A | ENSP00000406358.1:n.89+7G>A | |
| ENST00000466823.2:c.349+7G>A | ||
| ENST00000495568.7:n.564+7G>A | ||
| ENST00000497793.2:n.478+7G>A | ||
| NM_001142864.2:c.6323+7G>A | NP_001136336.2:n.6323+7G>A | |
| NM_001142864.3:c.6323+7G>A | NP_001136336.2:n.6323+7G>A | |
| NM_001142864.4:c.6323+7G>A MANE Select | NP_001136336.2:n.6323+7G>A |