Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73404220A= , CM000666.2:g.73404220A= | GRCh38 |
| NC_000004.11:g.74269937A= , CM000666.1:g.74269937A= | GRCh37 |
| NC_000004.10:g.74488801A= | NCBI36 |
| NG_009291.1:g.4966A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000441319.5:c.48-149A= | ENSP00000392541.1:n.48-149A= |