Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26519100C= , CM000664.2:g.26519100C= | GRCh38 |
| NC_000002.11:g.26741968C= , CM000664.1:g.26741968C= | GRCh37 |
| NC_000002.10:g.26595472C= | NCBI36 |
| NG_009937.1:g.44599G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000272371.7:c.237G= MANE Select | ENSP00000272371.2:p.Gly79= | |
| ENST00000272371.6:c.237G= | ENSP00000272371.2:p.Gly79= | |
| ENST00000403946.7:c.237G= | ENSP00000385255.3:p.Gly79= | |
| NM_001287489.1:c.237G= | NP_001274418.1:p.Gly79= | |
| NM_194248.2:c.237G= | NP_919224.1:p.Gly79= | |
| XM_005264644.2:c.237G= | XP_005264701.1:p.Gly79= | |
| XM_011533185.1:c.237G= | XP_011531487.1:p.Gly79= | |
| XM_017005338.1:c.237G= | XP_016860827.1:p.Gly79= | |
| NM_001287489.2:c.237G= | NP_001274418.1:p.Gly79= | |
| NM_194248.3:c.237G= MANE Select | NP_919224.1:p.Gly79= |