Linked Data
dbSNP Id:
rs1368805142
gnomAD v3:
16-88719535-C-A
gnomAD v4:
16-88719535-C-A
MyVariant Identifiers:
chr16:g.88785943C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88719535C>A , CM000678.2:g.88719535C>A | GRCh38 |
| NC_000016.9:g.88785943C>A , CM000678.1:g.88785943C>A | GRCh37 |
| NC_000016.8:g.87313444C>A | NCBI36 |
| NG_042229.1:g.70686G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301015.14:c.6471+39G>T MANE Select | ENSP00000301015.9:n.6471+39G>T | |
| ENST00000466823.3:c.497+39G>T | ||
| ENST00000301015.13:c.6471+39G>T | ENSP00000301015.9:n.6471+39G>T | |
| ENST00000419505.5:c.237+39G>T | ENSP00000406358.1:n.237+39G>T | |
| ENST00000466823.2:c.497+39G>T | ||
| ENST00000495568.7:n.712+39G>T | ||
| ENST00000497793.2:n.665G>T | ||
| NM_001142864.2:c.6471+39G>T | NP_001136336.2:n.6471+39G>T | |
| NM_001142864.3:c.6471+39G>T | NP_001136336.2:n.6471+39G>T | |
| NM_001142864.4:c.6471+39G>T MANE Select | NP_001136336.2:n.6471+39G>T |