Canonical Allele Identifier:
CA1657688861
Gene:
Linked Data
dbSNP Id:
rs1776569481
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.117450164A>G , CM000668.2:g.117450164A>G | GRCh38 |
| NC_000006.11:g.117771327A>G , CM000668.1:g.117771327A>G | GRCh37 |
| NC_000006.10:g.117878020A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000467125.1:c.547+116690T>C | ENSP00000487717.1:n.547+116690T>C |