Linked Data
gnomAD v4:
X-116173426-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.116173426A>G , CM000685.2:g.116173426A>G | GRCh38 |
| NC_000023.10:g.115304679A>G , CM000685.1:g.115304679A>G | GRCh37 |
| NC_000023.9:g.115218707A>G | NCBI36 |
| NG_016326.1:g.7722A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371906.5:c.*54A>G MANE Select | ENSP00000360973.4:n.*54A>G | |
| ENST00000680409.1:n.1614A>G | ||
| ENST00000371906.4:c.*54A>G | ENSP00000360973.4:n.*54A>G | |
| NM_000686.4:c.*54A>G | NP_000677.2:n.*54A>G | |
| XM_011537533.1:c.*54A>G | XP_011535835.1:n.*54A>G | |
| NM_000686.5:c.*54A>G MANE Select | NP_000677.2:n.*54A>G | |
| NM_001385624.1:c.*54A>G | NP_001372553.1:n.*54A>G |