Linked Data
gnomAD v4:
X-134498358-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.134498358G>C , CM000685.2:g.134498358G>C | GRCh38 |
| NC_000023.10:g.133632388G>C , CM000685.1:g.133632388G>C | GRCh37 |
| NC_000023.9:g.133460054G>C | NCBI36 |
| NG_012329.1:g.43214G>C | |
| NG_012329.2:g.43214G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298556.8:c.486-32G>C MANE Select | ENSP00000298556.7:n.486-32G>C | |
| ENST00000298556.7:c.486-32G>C | ENSP00000298556.7:n.486-32G>C | |
| ENST00000462974.5:n.644-32G>C | ||
| ENST00000475720.1:n.444-32G>C | ||
| NM_000194.2:c.486-32G>C | NP_000185.1:n.486-32G>C | |
| XM_011531328.1:c.504-32G>C | XP_011529630.1:n.504-32G>C | |
| NM_000194.3:c.486-32G>C MANE Select | NP_000185.1:n.486-32G>C |