Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38074947C>T , CM000664.2:g.38074947C>T | GRCh38 |
| NC_000002.11:g.38302090C>T , CM000664.1:g.38302090C>T | GRCh37 |
| NC_000002.10:g.38155594C>T | NCBI36 |
| NG_008386.2:g.6155G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000490576.2:c.442G>A | ENSP00000478839.2:p.Ala148Thr | |
| ENST00000610745.5:c.442G>A MANE Select | ENSP00000478561.1:p.Ala148Thr | |
| ENST00000494864.1:c.-70-3637G>A | ENSP00000479876.1:n.-70-3637G>A | |
| ENST00000610745.4:c.442G>A | ENSP00000478561.1:p.Ala148Thr | |
| ENST00000613082.1:n.376-539G>A | ||
| ENST00000614273.1:c.442G>A | ENSP00000483678.1:p.Ala148Thr | |
| NM_000104.3:c.442G>A | NP_000095.2:p.Ala148Thr | |
| NM_000104.4:c.442G>A MANE Select | NP_000095.2:p.Ala148Thr |