Linked Data
dbSNP Id:
rs1567771159
gnomAD v4:
16-89179460-C-G
MyVariant Identifiers:
chr16:g.89245868C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89179460C>G , CM000678.2:g.89179460C>G | GRCh38 |
| NC_000016.9:g.89245868C>G , CM000678.1:g.89245868C>G | GRCh37 |
| NC_000016.8:g.87773369C>G | NCBI36 |
| NG_012055.1:g.12706C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289746.3:c.87C>G MANE Select | ENSP00000289746.2:p.Thr29= | |
| ENST00000289746.2:c.87C>G | ENSP00000289746.2:p.Thr29= | |
| ENST00000521087.5:n.152C>G | ||
| ENST00000524089.1:n.152C>G | ||
| NM_004933.2:c.87C>G | NP_004924.1:p.Thr29= | |
| XM_011522806.1:c.87C>G | XP_011521108.1:p.Thr29= | |
| NM_004933.3:c.87C>G MANE Select | NP_004924.1:p.Thr29= |