Linked Data
dbSNP Id:
rs1790539914
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.80011513A>T , CM000669.2:g.80011513A>T | GRCh38 |
| NC_000007.13:g.79640829A>T , CM000669.1:g.79640829A>T | GRCh37 |
| NC_000007.12:g.79478765A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649225.1:c.-337+54447A>T | ENSP00000496829.1:n.-337+54447A>T |