Linked Data
gnomAD v4:
20-45547586-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.45547586G>T , CM000682.2:g.45547586G>T | GRCh38 |
| NC_000020.10:g.44176225G>T , CM000682.1:g.44176225G>T | GRCh37 |
| NC_000020.9:g.43609639G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651288.1:c.-229C>A (EPPIN-WFDC6) | ENSP00000498632.1:n.-229C>A | |
| ENST00000409554.1:c.-229C>A (EPPIN) | ENSP00000387153.1:n.-229C>A |