Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.123034456G= , CM000672.2:g.123034456G= | GRCh38 |
| NC_000010.10:g.124793972G= , CM000672.1:g.124793972G= | GRCh37 |
| NC_000010.9:g.124783962G= | NCBI36 |
| NG_008003.1:g.30544G= , LRG_451:g.30544G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358776.7:c.143G= MANE Select | ENSP00000357873.3:p.Gly48= | |
| ENST00000358776.6:c.143G= | ENSP00000357873.3:p.Gly48= | |
| ENST00000368869.8:c.-63G= | ENSP00000357862.4:n.-63G= | |
| ENST00000411816.2:n.160G= | ||
| NM_001609.3:c.143G= , LRG_451t1:c.143G= | NP_001600.1:p.Gly48= | |
| NM_001330174.1:c.-63G= | NP_001317103.1:n.-63G= | |
| NM_001330174.2:c.-63G= | NP_001317103.1:n.-63G= | |
| NM_001609.4:c.143G= MANE Select | NP_001600.1:p.Gly48= | |
| NM_001330174.3:c.-63G= | NP_001317103.1:n.-63G= |