Linked Data
gnomAD v4:
1-31373079-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.31373079C>T , CM000663.2:g.31373079C>T | GRCh38 |
| NC_000001.10:g.31845926C>T , CM000663.1:g.31845926C>T | GRCh37 |
| NC_000001.9:g.31618513C>T | NCBI36 |
| NG_047049.1:g.5205G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000482018.1:c.-27-38G>A | ENSP00000473982.1:n.-27-38G>A | |
| XM_011541007.1:c.-65G>A | XP_011539309.1:n.-65G>A | |
| NM_001320996.1:c.-65G>A | NP_001307925.1:n.-65G>A | |
| NM_004102.4:c.-65G>A | NP_004093.1:n.-65G>A | |
| XM_011541007.3:c.-65G>A | XP_011539309.1:n.-65G>A |