MyVariant.info:
GRCh38
chr12:g.64609189T>C
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.64609189T>C , CM000674.2:g.64609189T>C | GRCh38 |
| NC_000012.11:g.65002969T>C , CM000674.1:g.65002969T>C | GRCh37 |
| NC_000012.10:g.63289236T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000637125.1:c.294+67484T>C (RASSF3) | ENSP00000490100.1:n.294+67484T>C | |
| XR_945027.1:n.1024+156A>G (RASSF3-DT) | ||
| XR_945027.2:n.1045+156A>G (RASSF3-DT) |