Linked Data
gnomAD v4:
9-133352345-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133352345T>G , CM000671.2:g.133352345T>G | GRCh38 |
| NC_000009.10:g.135209021T>G | NCBI36 |
| NG_008477.1:g.9162A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371974.8:c.751+101A>C MANE Select | ENSP00000361042.3:n.751+101A>C | |
| ENST00000371974.7:c.751+101A>C | ENSP00000361042.3:n.751+101A>C | |
| ENST00000437995.1:n.661+101A>C | ||
| ENST00000495952.5:n.741+101A>C | ||
| ENST00000615505.4:c.424+101A>C | ENSP00000482067.1:n.424+101A>C | |
| NM_001280787.1:c.424+101A>C | NP_001267716.1:n.424+101A>C | |
| NM_003172.3:c.751+101A>C | NP_003163.1:n.751+101A>C | |
| XM_011518942.1:c.424+101A>C | XP_011517244.1:n.424+101A>C | |
| NM_003172.4:c.751+101A>C MANE Select | NP_003163.1:n.751+101A>C |