Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.29590660A>G , CM000679.2:g.29590660A>G | GRCh38 |
| NC_000017.10:g.27917678A>G , CM000679.1:g.27917678A>G | GRCh37 |
| NC_000017.9:g.24941804A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000487527.5:n.80+798A>G (ANKRD13B) | ||
| ENST00000583413.4:c.88+3282T>C (GIT1) | ENSP00000466824.1:n.88+3282T>C | |
| ENST00000583728.5:c.-283+798A>G (ANKRD13B) | ENSP00000467078.1:n.-283+798A>G | |
| XM_017024174.2:c.-283+798A>G (ANKRD13B) | XP_016879663.1:n.-283+798A>G |