Linked Data
MyVariant Identifiers:
chr17:g.64235865G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.66239747G>T , CM000679.2:g.66239747G>T | GRCh38 |
| NC_000017.10:g.64235865G>T , CM000679.1:g.64235865G>T | GRCh37 |
| NC_000017.9:g.61666327G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000577982.1:c.-43-10325C>A | ENSP00000464301.1:n.-43-10325C>A |