MyVariant.info:
GRCh37
chr12:g.54385599C>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.53991815C>G , CM000674.2:g.53991815C>G | GRCh38 |
| NC_000012.11:g.54385599C>G , CM000674.1:g.54385599C>G | GRCh37 |
| NC_000012.10:g.52671866C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504315.1:c.-193+1001C>G (HOXC6) | ENSP00000424124.1:n.-193+1001C>G | |
| ENST00000513209.1:c.166+5805C>G | ENSP00000476742.1:n.166+5805C>G | |
| NR_029617.1:n.78C>G (MIR196A2) |