gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.80180126C>A , CM000677.2:g.80180126C>A | GRCh38 |
| NC_000015.9:g.80472468C>A , CM000677.1:g.80472468C>A | GRCh37 |
| NC_000015.8:g.78259523C>A | NCBI36 |
| NG_012833.1:g.32128C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682012.1:n.1052C>A | ||
| ENST00000561421.6:c.963C>A MANE Select | ENSP00000453347.2:p.Tyr321Ter | |
| ENST00000646551.1:n.2577C>A | ||
| ENST00000261755.9:c.963C>A | ENSP00000261755.5:p.Tyr321Ter | |
| ENST00000407106.5:c.963C>A | ENSP00000385080.1:p.Tyr321Ter | |
| ENST00000539156.5:c.753C>A | ENSP00000454271.1:p.Tyr251Ter | |
| ENST00000559217.1:n.180C>A | ||
| ENST00000561353.2:c.61C>A | ||
| ENST00000561421.5:c.963C>A | ENSP00000453347.1:p.Tyr321Ter | |
| NM_000137.2:c.963C>A | NP_000128.1:p.Tyr321Ter | |
| XM_024449872.1:c.963C>A | XP_024305640.1:p.Tyr321Ter | |
| NM_000137.4:c.963C>A MANE Select | NP_000128.1:p.Tyr321Ter | |
| NM_001374377.1:c.963C>A | NP_001361306.1:p.Tyr321Ter | |
| NM_001374380.1:c.963C>A | NP_001361309.1:p.Tyr321Ter |