Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.88008238G= , CM000666.2:g.88008238G= | GRCh38 |
| NC_000004.11:g.88929390G= , CM000666.1:g.88929390G= | GRCh37 |
| NC_000004.10:g.89148414G= | NCBI36 |
| NG_008604.1:g.5571G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237596.7:c.505G= MANE Select | ENSP00000237596.2:p.Gly169= | |
| ENST00000237596.6:c.505G= | ENSP00000237596.2:p.Gly169= | |
| ENST00000506727.1:n.7G= | ||
| NM_000297.3:c.505G= | NP_000288.1:p.Gly169= | |
| XM_011532028.1:c.505G= | XP_011530330.1:p.Gly169= | |
| XR_244632.2:n.600G= | ||
| NR_156488.1:n.592G= | ||
| XM_011532028.2:c.505G= | XP_011530330.1:p.Gly169= | |
| NM_000297.4:c.505G= MANE Select | NP_000288.1:p.Gly169= | |
| NR_156488.2:n.604G= |