Linked Data
gnomAD v4:
14-20454895-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.20454895C>A , CM000676.2:g.20454895C>A | GRCh38 |
| NC_000014.8:g.20923054C>A , CM000676.1:g.20923054C>A | GRCh37 |
| NC_000014.7:g.19992894C>A | NCBI36 |
| NG_008718.1:g.4765C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000206542.8:c.-212G>T | ENSP00000206542.4:n.-212G>T | |
| ENST00000556252.1:n.159G>T | ||
| ENST00000556439.1:n.195G>T | ||
| NM_017807.3:c.-212G>T | NP_060277.1:n.-212G>T | |
| XM_011536930.1:c.-273G>T | XP_011535232.1:n.-273G>T |