Canonical Allele Identifier:
CA1657688854
Gene:
Linked Data
dbSNP Id:
rs1776569387
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.117450149A>C , CM000668.2:g.117450149A>C | GRCh38 |
| NC_000006.11:g.117771312A>C , CM000668.1:g.117771312A>C | GRCh37 |
| NC_000006.10:g.117878005A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000467125.1:c.547+116705T>G | ENSP00000487717.1:n.547+116705T>G |