Canonical Allele Identifier:
CA1672978985
Gene:
Linked Data
dbSNP Id:
rs1777185084
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151633425A>T , CM000668.2:g.151633425A>T | GRCh38 |
| NC_000006.11:g.151954560A>T , CM000668.1:g.151954560A>T | GRCh37 |
| NC_000006.10:g.151996253A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943115.1:n.2496+3443A>T |