Linked Data
ClinVar Variation Id:
325714
ClinVar RCV Id:
RCV000306411
dbSNP Id:
rs143084065
gnomAD v2:
17-76993995-G-A
gnomAD v3:
17-78997913-G-A
gnomAD v4:
17-78997913-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.78997913G>A , CM000679.2:g.78997913G>A | GRCh38 |
| NC_000017.10:g.76993995G>A , CM000679.1:g.76993995G>A | GRCh37 |
| NC_000017.9:g.74505590G>A | NCBI36 |
| NG_016645.1:g.16905C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392446.10:c.-96C>T MANE Select | ENSP00000376241.4:n.-96C>T | |
| ENST00000302345.6:c.-291C>T | ENSP00000307674.2:n.-291C>T | |
| ENST00000392446.9:c.-96C>T | ENSP00000376241.4:n.-96C>T | |
| ENST00000586916.6:c.-96C>T | ENSP00000467970.1:n.-96C>T | |
| ENST00000588075.5:c.-291C>T | ENSP00000465769.1:n.-291C>T | |
| ENST00000588611.5:c.-96C>T | ENSP00000465816.1:n.-96C>T | |
| ENST00000590370.5:c.-96C>T | ENSP00000466637.1:n.-96C>T | |
| ENST00000591625.5:c.-291C>T | ENSP00000467777.1:n.-291C>T | |
| ENST00000591773.5:c.-96C>T | ENSP00000467437.1:n.-96C>T | |
| ENST00000591811.1:c.-96C>T | ENSP00000464841.1:n.-96C>T | |
| ENST00000592033.5:c.-96C>T | ENSP00000467886.1:n.-96C>T | |
| ENST00000592228.1:c.-22-269C>T | ENSP00000466743.1:n.-22-269C>T | |
| ENST00000592887.1:n.308C>T | ||
| ENST00000620915.4:c.-152-139C>T | ENSP00000477798.1:n.-152-139C>T | |
| NM_001159772.1:c.-96C>T | NP_001153244.1:n.-96C>T | |
| NM_001159773.1:c.-96C>T | NP_001153245.1:n.-96C>T | |
| NM_138793.3:c.-291C>T | NP_620148.1:n.-291C>T | |
| XM_005257020.1:c.-291C>T | XP_005257077.1:n.-291C>T | |
| XM_005257021.1:c.-291C>T | XP_005257078.1:n.-291C>T | |
| XM_005257022.1:c.-96C>T | XP_005257079.1:n.-96C>T | |
| XM_006721683.1:c.-96C>T | XP_006721746.1:n.-96C>T | |
| XM_011524291.1:c.-291C>T | XP_011522593.1:n.-291C>T | |
| XM_011524292.1:c.-291C>T | XP_011522594.1:n.-291C>T | |
| XM_011524293.1:c.-291C>T | XP_011522595.1:n.-291C>T | |
| XM_011524294.1:c.-96C>T | XP_011522596.1:n.-96C>T | |
| XM_011524295.1:c.-96C>T | XP_011522597.1:n.-96C>T | |
| XM_011524294.2:c.-96C>T | XP_011522596.1:n.-96C>T | |
| XM_011524295.2:c.-96C>T | XP_011522597.1:n.-96C>T | |
| XM_024450564.1:c.-291C>T | XP_024306332.1:n.-291C>T | |
| XR_001752424.2:n.154C>T | ||
| NM_001159773.2:c.-96C>T MANE Select | NP_001153245.1:n.-96C>T | |
| NM_001159772.2:c.-96C>T | NP_001153244.1:n.-96C>T | |
| NM_138793.4:c.-291C>T | NP_620148.1:n.-291C>T |