Linked Data
gnomAD v4:
X-134493367-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.134493367A>T , CM000685.2:g.134493367A>T | GRCh38 |
| NC_000023.10:g.133627397A>T , CM000685.1:g.133627397A>T | GRCh37 |
| NC_000023.9:g.133455063A>T | NCBI36 |
| NG_012329.1:g.38223A>T | |
| NG_012329.2:g.38223A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298556.8:c.403-141A>T MANE Select | ENSP00000298556.7:n.403-141A>T | |
| ENST00000298556.7:c.403-141A>T | ENSP00000298556.7:n.403-141A>T | |
| ENST00000462974.5:n.561-141A>T | ||
| ENST00000475720.1:n.361-141A>T | ||
| NM_000194.2:c.403-141A>T | NP_000185.1:n.403-141A>T | |
| XM_011531328.1:c.421-141A>T | XP_011529630.1:n.421-141A>T | |
| NM_000194.3:c.403-141A>T MANE Select | NP_000185.1:n.403-141A>T |