Canonical Allele Identifier:
CA1697889707
Gene:
Linked Data
dbSNP Id:
rs1790896228
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.30897497C>T , CM000669.2:g.30897497C>T | GRCh38 |
| NC_000007.13:g.30937112C>T , CM000669.1:g.30937112C>T | GRCh37 |
| NC_000007.12:g.30903637C>T | NCBI36 |
| NG_007475.2:g.49104C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000509504.2:c.622-14496C>T |