Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43755620C= , CM000679.2:g.43755620C= | GRCh38 |
| NC_000017.10:g.41832988C= , CM000679.1:g.41832988C= | GRCh37 |
| NC_000017.9:g.39188514C= | NCBI36 |
| NG_008078.2:g.8169G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000301691.3:c.364G= MANE Select | ENSP00000301691.1:p.Gly122= | |
| ENST00000301691.2:c.364G= | ENSP00000301691.1:p.Gly122= | |
| NM_025237.2:c.364G= | NP_079513.1:p.Gly122= | |
| NM_025237.3:c.364G= MANE Select | NP_079513.1:p.Gly122= |