Linked Data
dbSNP Id:
rs1577490868
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.35981538A>T , CM000666.2:g.35981538A>T | GRCh38 |
| NC_000004.11:g.35983160A>T , CM000666.1:g.35983160A>T | GRCh37 |
| NC_000004.10:g.35659555A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000503225.5:n.1607+3692T>A | ||
| XR_925192.1:n.1411T>A |