Linked Data
gnomAD v4:
4-121696977-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.121696977G>C , CM000666.2:g.121696977G>C | GRCh38 |
| NC_000004.11:g.122618132G>C , CM000666.1:g.122618132G>C | GRCh37 |
| NC_000004.10:g.122837582G>C | NCBI36 |
| NG_032042.1:g.5016C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000296511.10:c.-150C>G MANE Select | ENSP00000296511.5:n.-150C>G | |
| ENST00000296511.9:c.-150C>G | ENSP00000296511.5:n.-150C>G | |
| ENST00000509016.5:n.16C>G | ||
| ENST00000513428.5:n.16C>G | ||
| ENST00000513523.1:n.19C>G | ||
| NM_001154.3:c.-150C>G | NP_001145.1:n.-150C>G | |
| XM_017008141.2:c.-150C>G | XP_016863630.1:n.-150C>G | |
| NM_001154.4:c.-150C>G MANE Select | NP_001145.1:n.-150C>G |