Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10629660C>T , CM000679.2:g.10629660C>T | GRCh38 |
| NC_000017.10:g.10532977C>T , CM000679.1:g.10532977C>T | GRCh37 |
| NC_000017.9:g.10473702C>T | NCBI36 |
| NG_011537.1:g.32639G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002470.4:c.5733G>A MANE Select | NP_002461.2:p.Ala1911= |
| ENST00000583535.6:c.5733G>A MANE Select | ENSP00000464317.1:p.Ala1911= |
| NM_002470.3:c.5733G>A | NP_002461.2:p.Ala1911= |
| ENST00000577963.1:n.275G>A | |
| ENST00000579928.2:n.263G>A | |
| ENST00000583535.5:c.5733G>A | ENSP00000464317.1:p.Ala1911= |
| XM_011523870.1:c.5733G>A | XP_011522172.1:p.Ala1911= |
| XM_011523870.3:c.5733G>A | XP_011522172.1:p.Ala1911= |
| XM_011523871.1:c.5733G>A | XP_011522173.1:p.Ala1911= |
| XM_011523871.2:c.5733G>A | XP_011522173.1:p.Ala1911= |