Linked Data
gnomAD v4:
14-96204928-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.96204928C>A , CM000676.2:g.96204928C>A | GRCh38 |
| NC_000014.8:g.96671265C>A , CM000676.1:g.96671265C>A | GRCh37 |
| NC_000014.7:g.95741018C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000554311.2:c.-71C>A MANE Select | ENSP00000450482.1:n.-71C>A | |
| ENST00000539359.1:c.-313C>A | ENSP00000438376.1:n.-313C>A | |
| ENST00000542454.2:c.-2839C>A | ENSP00000439459.2:n.-2839C>A | |
| ENST00000553811.1:c.-66C>A | ENSP00000450984.1:n.-66C>A | |
| ENST00000554311.1:c.-71C>A | ENSP00000450482.1:n.-71C>A | |
| NM_000623.3:c.-66C>A | NP_000614.1:n.-66C>A | |
| NM_000623.4:c.-66C>A | NP_000614.1:n.-66C>A | |
| NM_001379692.1:c.-71C>A MANE Select | NP_001366621.1:n.-71C>A |