Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312737A= , CM000673.2:g.118312737A= | GRCh38 |
| NC_000011.9:g.118183452A= , CM000673.1:g.118183452A= | GRCh37 |
| NC_000011.8:g.117688662A= | NCBI36 |
| NG_007383.1:g.13158A= , LRG_38:g.13158A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.223A= MANE Select | ENSP00000354566.4:p.Ile75= | |
| ENST00000361763.8:c.223A= | ENSP00000354566.4:p.Ile75= | |
| ENST00000526146.5:n.769A= | ||
| ENST00000528435.5:n.776A= | ||
| ENST00000528600.1:c.205A= | ENSP00000433975.1:p.Ile69= | |
| ENST00000529713.5:n.329A= | ||
| ENST00000531913.1:n.594A= | ||
| NM_000733.3:c.223A= , LRG_38t1:c.223A= | NP_000724.1:p.Ile75= | |
| NM_000733.4:c.223A= MANE Select | NP_000724.1:p.Ile75= |