Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.155140012G>A , CM000663.2:g.155140012G>A | GRCh38 |
| NC_000001.10:g.155112488G>A , CM000663.1:g.155112488G>A | GRCh37 |
| NC_000001.9:g.153379112G>A | NCBI36 |
| NG_012871.1:g.5509C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368400.5:c.229C>T MANE Select | ENSP00000357385.5:p.Gln77Ter | |
| ENST00000341298.3:c.229C>T | ENSP00000344338.3:p.Gln77Ter | |
| ENST00000368399.1:c.319C>T | ENSP00000357384.1:p.Gln107Ter | |
| ENST00000368400.4:c.229C>T | ENSP00000357385.4:p.Gln77Ter | |
| NM_018973.3:c.319C>T | NP_061846.2:p.Gln107Ter | |
| NM_153741.1:c.229C>T | NP_714963.1:p.Gln77Ter | |
| XM_017001498.1:c.229C>T | XP_016856987.1:p.Gln77Ter | |
| NM_153741.2:c.229C>T MANE Select | NP_714963.1:p.Gln77Ter | |
| NM_018973.4:c.319C>T | NP_061846.2:p.Gln107Ter |