Canonical Allele Identifier:
CA422484748
Gene:
Linked Data
MyVariant Identifiers:
chr1:g.192769792T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.192800662T>A , CM000663.2:g.192800662T>A | GRCh38 |
| NC_000001.10:g.192769792T>A , CM000663.1:g.192769792T>A | GRCh37 |
| NC_000001.9:g.191036415T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429211.2:n.92T>A |