Linked Data
gnomAD v4:
4-121696981-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.121696981G>A , CM000666.2:g.121696981G>A | GRCh38 |
| NC_000004.11:g.122618136G>A , CM000666.1:g.122618136G>A | GRCh37 |
| NC_000004.10:g.122837586G>A | NCBI36 |
| NG_032042.1:g.5012C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000296511.9:c.-154C>T | ENSP00000296511.5:n.-154C>T | |
| ENST00000509016.5:n.12C>T | ||
| ENST00000513428.5:n.12C>T | ||
| ENST00000513523.1:n.15C>T | ||
| NM_001154.3:c.-154C>T | NP_001145.1:n.-154C>T | |
| XM_017008141.2:c.-154C>T | XP_016863630.1:n.-154C>T |