Linked Data
gnomAD v4:
11-89178369-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.89178369C>A , CM000673.2:g.89178369C>A | GRCh38 |
| NC_000011.9:g.88911537C>A , CM000673.1:g.88911537C>A | GRCh37 |
| NC_000011.8:g.88551185C>A | NCBI36 |
| NG_008748.1:g.5498C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263321.6:c.416C>A MANE Select | ENSP00000263321.4:p.Thr139Asn | |
| ENST00000263321.5:c.416C>A | ENSP00000263321.4:p.Thr139Asn | |
| ENST00000526139.1:n.477C>A | ||
| NM_000372.4:c.416C>A | NP_000363.1:p.Thr139Asn | |
| XM_011542970.1:c.416C>A | XP_011541272.1:p.Thr139Asn | |
| XM_011542970.2:c.416C>A | XP_011541272.1:p.Thr139Asn | |
| XR_001748321.1:n.2718-64836G>T | ||
| XR_001748322.1:n.2733-64836G>T | ||
| NM_000372.5:c.416C>A MANE Select | NP_000363.1:p.Thr139Asn |