Canonical Allele Identifier:
CA476840368
Gene:
Linked Data
MyVariant Identifiers:
chr11:g.114231374G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.114360652G>T , CM000673.2:g.114360652G>T | GRCh38 |
| NC_000011.9:g.114231374G>T , CM000673.1:g.114231374G>T | GRCh37 |
| NC_000011.8:g.113736584G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_120567.1:n.3814C>A |