Canonical Allele Identifier:
CA1697889716
Gene:
Linked Data
dbSNP Id:
rs1790896456
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.30897506C>T , CM000669.2:g.30897506C>T | GRCh38 |
| NC_000007.13:g.30937121C>T , CM000669.1:g.30937121C>T | GRCh37 |
| NC_000007.12:g.30903646C>T | NCBI36 |
| NG_007475.2:g.49113C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000509504.2:c.622-14487C>T |