Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.91055467T>C , CM000674.2:g.91055467T>C | GRCh38 |
| NC_000012.11:g.91449244T>C , CM000674.1:g.91449244T>C | GRCh37 |
| NC_000012.10:g.89973375T>C | NCBI36 |
| NG_021223.1:g.7888A>G , LRG_538:g.7888A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266719.4:c.815A>G MANE Select | ENSP00000266719.3:p.Asn272Ser | |
| ENST00000266719.3:c.815A>G | ENSP00000266719.3:p.Asn272Ser | |
| NM_007035.3:c.815A>G , LRG_538t1:c.815A>G | NP_008966.1:p.Asn272Ser | |
| XM_011537781.1:c.815A>G | XP_011536083.1:p.Asn272Ser | |
| NM_007035.4:c.815A>G MANE Select | NP_008966.1:p.Asn272Ser |