Canonical Allele Identifier:
CA422484594
Gene:
Linked Data
MyVariant Identifiers:
chr1:g.192769765A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.192800635A>T , CM000663.2:g.192800635A>T | GRCh38 |
| NC_000001.10:g.192769765A>T , CM000663.1:g.192769765A>T | GRCh37 |
| NC_000001.9:g.191036388A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429211.2:n.65A>T |