Linked Data
dbSNP Id:
rs1266111063
gnomAD v2:
4-157892889-C-T
gnomAD v3:
4-156971737-C-T
gnomAD v4:
4-156971737-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.156971737C>T , CM000666.2:g.156971737C>T | GRCh38 |
| NC_000004.11:g.157892889C>T , CM000666.1:g.157892889C>T | GRCh37 |
| NC_000004.10:g.158112339C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502773.6:c.-834G>A MANE Select | ENSP00000422464.1:n.-834G>A | |
| NM_016205.3:c.-834G>A MANE Select | NP_057289.1:n.-834G>A | |
| NR_036641.2:n.63G>A |