dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10403483G>C , CM000681.2:g.10403483G>C | GRCh38 |
| NC_000019.9:g.10514159G>C , CM000681.1:g.10514159G>C | GRCh37 |
| NC_000019.8:g.10375159G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222005.7:c.-4C>G (CDC37) MANE Select | ENSP00000222005.1:n.-4C>G | |
| ENST00000222005.6:c.-4C>G (CDC37) | ENSP00000222005.1:n.-4C>G | |
| ENST00000588869.1:c.-4C>G (CDC37) | ENSP00000464971.1:n.-4C>G | |
| ENST00000589629.5:c.-4C>G (CDC37) | ENSP00000467747.1:n.-4C>G | |
| ENST00000591248.5:n.48C>G (CDC37) | ||
| ENST00000593124.1:c.-4C>G (CDC37) | ENSP00000465724.1:n.-4C>G | |
| NM_007065.3:c.-4C>G (CDC37) | NP_008996.1:n.-4C>G | |
| NR_031592.1:n.56C>G (MIR1181) | ||
| XM_011527652.1:c.-4C>G (CDC37) | XP_011525954.1:n.-4C>G | |
| XM_011527652.3:c.-4C>G (CDC37) | XP_011525954.1:n.-4C>G | |
| NM_007065.4:c.-4C>G (CDC37) MANE Select | NP_008996.1:n.-4C>G |