Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.49440273C= , CM000668.2:g.49440273C= | GRCh38 |
| NC_000006.11:g.49407986C= , CM000668.1:g.49407986C= | GRCh37 |
| NC_000006.10:g.49515945C= | NCBI36 |
| NG_007100.1:g.27867G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000255.4:c.1889G= MANE Select | NP_000246.2:p.Gly630= |
| ENST00000274813.4:c.1889G= MANE Select | ENSP00000274813.3:p.Gly630= |
| NM_000255.3:c.1889G= | NP_000246.2:p.Gly630= |
| ENST00000274813.3:c.1889G= | ENSP00000274813.3:p.Gly630= |
| XM_005249143.2:c.1889G= | XP_005249200.1:p.Gly630= |
| XM_005249143.3:c.1889G= | XP_005249200.1:p.Gly630= |