Canonical Allele Identifier:
CA2699207857
Gene:
Linked Data
dbSNP Id:
rs2103837837
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.41534684C>T , CM000664.2:g.41534684C>T | GRCh38 |
| NC_000002.11:g.41761824C>T , CM000664.1:g.41761824C>T | GRCh37 |
| NC_000002.10:g.41615328C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_939996.1:n.181+3042G>A | ||
| XR_939997.1:n.146+3042G>A | ||
| XR_939997.2:n.9529+3042G>A |