Linked Data
gnomAD v4:
X-116172187-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.116172187A>T , CM000685.2:g.116172187A>T | GRCh38 |
| NC_000023.10:g.115303440A>T , CM000685.1:g.115303440A>T | GRCh37 |
| NC_000023.9:g.115217468A>T | NCBI36 |
| NG_016326.1:g.6483A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371906.5:c.-35-59A>T MANE Select | ENSP00000360973.4:n.-35-59A>T | |
| ENST00000680409.1:n.375A>T | ||
| ENST00000681852.1:c.-35-59A>T | ENSP00000505750.1:n.-35-59A>T | |
| ENST00000371906.4:c.-35-59A>T | ENSP00000360973.4:n.-35-59A>T | |
| NM_000686.4:c.-35-59A>T | NP_000677.2:n.-35-59A>T | |
| XM_011537533.1:c.-35-59A>T | XP_011535835.1:n.-35-59A>T | |
| NM_000686.5:c.-35-59A>T MANE Select | NP_000677.2:n.-35-59A>T | |
| NM_001385624.1:c.-35-59A>T | NP_001372553.1:n.-35-59A>T |