Canonical Allele Identifier:
CA1619157051
Gene:
Linked Data
dbSNP Id:
rs1562286139
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31439731T>C , CM000668.2:g.31439731T>C | GRCh38 |
| NC_000006.11:g.31407508T>C , CM000668.1:g.31407508T>C | GRCh37 |
| NC_000006.10:g.31515487T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_926694.1:n.376A>G |