Linked Data
gnomAD v4:
4-121696980-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.121696980T>G , CM000666.2:g.121696980T>G | GRCh38 |
| NC_000004.11:g.122618135T>G , CM000666.1:g.122618135T>G | GRCh37 |
| NC_000004.10:g.122837585T>G | NCBI36 |
| NG_032042.1:g.5013A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000296511.10:c.-153A>C MANE Select | ENSP00000296511.5:n.-153A>C | |
| ENST00000296511.9:c.-153A>C | ENSP00000296511.5:n.-153A>C | |
| ENST00000509016.5:n.13A>C | ||
| ENST00000513428.5:n.13A>C | ||
| ENST00000513523.1:n.16A>C | ||
| NM_001154.3:c.-153A>C | NP_001145.1:n.-153A>C | |
| XM_017008141.2:c.-153A>C | XP_016863630.1:n.-153A>C | |
| NM_001154.4:c.-153A>C MANE Select | NP_001145.1:n.-153A>C |