Linked Data
gnomAD v4:
4-121696978-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.121696978A>G , CM000666.2:g.121696978A>G | GRCh38 |
| NC_000004.11:g.122618133A>G , CM000666.1:g.122618133A>G | GRCh37 |
| NC_000004.10:g.122837583A>G | NCBI36 |
| NG_032042.1:g.5015T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000296511.10:c.-151T>C MANE Select | ENSP00000296511.5:n.-151T>C | |
| ENST00000296511.9:c.-151T>C | ENSP00000296511.5:n.-151T>C | |
| ENST00000509016.5:n.15T>C | ||
| ENST00000513428.5:n.15T>C | ||
| ENST00000513523.1:n.18T>C | ||
| NM_001154.3:c.-151T>C | NP_001145.1:n.-151T>C | |
| XM_017008141.2:c.-151T>C | XP_016863630.1:n.-151T>C | |
| NM_001154.4:c.-151T>C MANE Select | NP_001145.1:n.-151T>C |