Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48459793A= , CM000675.2:g.48459793A= | GRCh38 |
| NC_000013.10:g.49033929A= , CM000675.1:g.49033929A= | GRCh37 |
| NC_000013.9:g.47931930A= | NCBI36 |
| NG_009009.1:g.161047A= , LRG_517:g.161047A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.2066A= MANE Select | ENSP00000267163.4:p.Gln689= | |
| ENST00000643064.1:c.194+78350A= | ||
| ENST00000650461.1:c.2066A= | ENSP00000497193.1:p.Gln689= | |
| ENST00000267163.4:c.2066A= | ENSP00000267163.4:p.Gln689= | |
| NM_000321.2:c.2066A= , LRG_517t1:c.2066A= | NP_000312.2:p.Gln689= | |
| XM_011535171.1:c.1805A= | XP_011533473.1:p.Gln602= | |
| XM_011535171.2:c.1805A= | XP_011533473.1:p.Gln602= | |
| NM_000321.3:c.2066A= MANE Select | NP_000312.2:p.Gln689= |