Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.130381162G>A , CM000669.2:g.130381162G>A | GRCh38 |
| NC_000007.13:g.130021003G>A , CM000669.1:g.130021003G>A | GRCh37 |
| NC_000007.12:g.129808239G>A | NCBI36 |
| NG_042276.1:g.5792G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001868.4:c.130G>A MANE Select | NP_001859.1:p.Asp44Asn |
| ENST00000011292.8:c.130G>A MANE Select | ENSP00000011292.3:p.Asp44Asn |
| NM_001868.3:c.130G>A | NP_001859.1:p.Asp44Asn |
| ENST00000011292.7:c.130G>A | ENSP00000011292.3:p.Asp44Asn |
| ENST00000476062.5:c.-135G>A | ENSP00000419408.1:n.-135G>A |
| ENST00000481342.5:c.-135G>A | ENSP00000420218.1:n.-135G>A |
| ENST00000484324.1:c.-135G>A | ENSP00000419497.1:n.-135G>A |
| ENST00000491460.5:n.157G>A | |
| ENST00000604896.5:c.141+16G>A | ENSP00000475021.1:n.141+16G>A |