Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52027986A= , CM000666.2:g.52027986A= | GRCh38 |
| NC_000004.11:g.52894152A= , CM000666.1:g.52894152A= | GRCh37 |
| NC_000004.10:g.52588909A= | NCBI36 |
| NG_008891.1:g.15334T= , LRG_204:g.15334T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.735T= MANE Select | ENSP00000370839.6:p.Gly245= | |
| ENST00000381431.9:c.735T= | ENSP00000370839.5:p.Gly245= | |
| NM_000232.4:c.735T= , LRG_204t1:c.735T= | NP_000223.1:p.Gly245= | |
| XM_006714049.2:c.438T= | XP_006714112.1:p.Gly146= | |
| XM_011534403.1:c.525T= | XP_011532705.1:p.Gly175= | |
| XM_011534404.1:c.438T= | XP_011532706.1:p.Gly146= | |
| NM_000232.5:c.735T= MANE Select | NP_000223.1:p.Gly245= |