Linked Data
dbSNP Id:
rs1660442859
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.241847967A>T , CM000663.2:g.241847967A>T | GRCh38 |
| NC_000001.10:g.242011269A>T , CM000663.1:g.242011269A>T | GRCh37 |
| NC_000001.9:g.240077892A>T | NCBI36 |
| NG_029100.1:g.4777A>T | |
| NG_029100.2:g.4777A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000519225.5:c.-548A>T | ENSP00000429720.1:n.-548A>T | |
| XM_011544322.1:c.-548A>T | XP_011542624.1:n.-548A>T |