Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.188984824A>C , CM000664.2:g.188984824A>C | GRCh38 |
| NC_000002.11:g.189849550A>C , CM000664.1:g.189849550A>C | GRCh37 |
| NC_000002.10:g.189557795A>C | NCBI36 |
| NG_007404.1:g.15452A>C , LRG_3:g.15452A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000090.4:c.144A>C MANE Select | NP_000081.2:p.Glu48Asp |
| ENST00000304636.9:c.144A>C MANE Select | ENSP00000304408.4:p.Glu48Asp |
| NM_000090.3:c.144A>C , LRG_3t1:c.144A>C | NP_000081.1:p.Glu48Asp |
| ENST00000304636.7:c.144A>C | ENSP00000304408.3:p.Glu48Asp |
| ENST00000317840.9:c.144A>C | ENSP00000315243.6:p.Glu48Asp |
| ENST00000450867.2:c.144A>C | ENSP00000415346.2:p.Glu48Asp |
| ENST00000470167.1:n.240A>C |