Linked Data
gnomAD v4:
14-91272526-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272526A>G , CM000676.2:g.91272526A>G | GRCh38 |
| NC_000014.8:g.91738870A>G , CM000676.1:g.91738870A>G | GRCh37 |
| NC_000014.7:g.90808623A>G | NCBI36 |
| NG_033118.1:g.150319T>C | |
| NG_033118.2:g.150319T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.*99T>C MANE Select | ENSP00000374507.6:n.*99T>C | |
| ENST00000331194.8:c.*99T>C | ENSP00000330332.8:n.*99T>C | |
| ENST00000389857.10:c.*99T>C | ENSP00000374507.6:n.*99T>C | |
| ENST00000556726.5:c.2414T>C | ||
| NM_001080414.3:c.*99T>C | NP_001073883.2:n.*99T>C | |
| XM_011536796.1:c.*99T>C | XP_011535098.1:n.*99T>C | |
| XM_011536796.2:c.*99T>C | XP_011535098.1:n.*99T>C | |
| XM_017021336.1:c.*99T>C | XP_016876825.1:n.*99T>C | |
| NM_001080414.4:c.*99T>C MANE Select | NP_001073883.2:n.*99T>C |