Canonical Allele Identifier:
CA422484622
Gene:
Linked Data
MyVariant Identifiers:
chr1:g.192769770T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.192800640T>G , CM000663.2:g.192800640T>G | GRCh38 |
| NC_000001.10:g.192769770T>G , CM000663.1:g.192769770T>G | GRCh37 |
| NC_000001.9:g.191036393T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429211.2:n.70T>G |