Linked Data
gnomAD v4:
X-134493441-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.134493441T>G , CM000685.2:g.134493441T>G | GRCh38 |
| NC_000023.10:g.133627471T>G , CM000685.1:g.133627471T>G | GRCh37 |
| NC_000023.9:g.133455137T>G | NCBI36 |
| NG_012329.1:g.38297T>G | |
| NG_012329.2:g.38297T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298556.8:c.403-67T>G MANE Select | ENSP00000298556.7:n.403-67T>G | |
| ENST00000298556.7:c.403-67T>G | ENSP00000298556.7:n.403-67T>G | |
| ENST00000462974.5:n.561-67T>G | ||
| ENST00000475720.1:n.361-67T>G | ||
| NM_000194.2:c.403-67T>G | NP_000185.1:n.403-67T>G | |
| XM_011531328.1:c.421-67T>G | XP_011529630.1:n.421-67T>G | |
| NM_000194.3:c.403-67T>G MANE Select | NP_000185.1:n.403-67T>G |