Linked Data
MyVariant Identifiers:
chr12:g.56435448C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56041664C>G , CM000674.2:g.56041664C>G | GRCh38 |
| NC_000012.11:g.56435448C>G , CM000674.1:g.56435448C>G | GRCh37 |
| NC_000012.10:g.54721715C>G | NCBI36 |
| NG_023201.1:g.4763C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356464.10:c.-356-147C>G | ENSP00000348849.5:n.-356-147C>G | |
| XR_944989.1:n.49G>C | ||
| XR_944990.1:n.49G>C | ||
| XR_944989.3:n.340G>C | ||
| XR_944990.3:n.340G>C |