Canonical Allele Identifier:
CA1247519133
Gene:
Linked Data
dbSNP Id:
rs1667991764
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.41534670C>T , CM000664.2:g.41534670C>T | GRCh38 |
| NC_000002.11:g.41761810C>T , CM000664.1:g.41761810C>T | GRCh37 |
| NC_000002.10:g.41615314C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_939996.1:n.181+3056G>A | ||
| XR_939997.1:n.146+3056G>A | ||
| XR_939997.2:n.9529+3056G>A |