Linked Data
ClinVar Variation Id:
733616
ClinVar RCV Id:
RCV000908935
dbSNP Id:
rs56688069
ExAC:
16:16248477 G / A
gnomAD v2:
16-16248477-G-A
gnomAD v3:
16-16154620-G-A
gnomAD v4:
16-16154620-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16154620G>A , CM000678.2:g.16154620G>A | GRCh38 |
| NC_000016.9:g.16248477G>A , CM000678.1:g.16248477G>A | GRCh37 |
| NC_000016.8:g.16155978G>A | NCBI36 |
| NG_007558.2:g.73852C>T | |
| NG_007558.3:g.73998C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622290.5:c.*380+8C>T | ENSP00000483331.2:n.*380+8C>T | |
| ENST00000205557.12:c.4208+8C>T MANE Select | ENSP00000205557.7:n.4208+8C>T | |
| ENST00000640696.1:c.1022+8C>T | ENSP00000492197.1:n.1022+8C>T | |
| ENST00000205557.11:c.4208+8C>T | ENSP00000205557.7:n.4208+8C>T | |
| ENST00000456970.6:c.3833+8C>T | ENSP00000405002.2:n.3833+8C>T | |
| ENST00000576204.5:n.1071+8C>T | ||
| ENST00000622290.4:c.*1417+8C>T | ENSP00000483331.1:n.*1417+8C>T | |
| NM_001171.5:c.4208+8C>T | NP_001162.4:n.4208+8C>T | |
| XM_011522479.1:c.4175+8C>T | XP_011520781.1:n.4175+8C>T | |
| XM_011522480.1:c.3866+8C>T | XP_011520782.1:n.3866+8C>T | |
| XM_011522481.1:c.3866+8C>T | XP_011520783.1:n.3866+8C>T | |
| XR_933134.1:n.539-5161G>A | ||
| NM_001351800.1:c.3866+8C>T | NP_001338729.1:n.3866+8C>T | |
| NR_147784.1:n.3870+8C>T | ||
| XM_011522479.2:c.4175+8C>T | XP_011520781.1:n.4175+8C>T | |
| XM_011522481.3:c.3866+8C>T | XP_011520783.1:n.3866+8C>T | |
| XM_017023212.1:c.4040+8C>T | XP_016878701.1:n.4040+8C>T | |
| XM_024450261.1:c.4244+8C>T | XP_024306029.1:n.4244+8C>T | |
| NM_001171.6:c.4208+8C>T MANE Select | NP_001162.5:n.4208+8C>T |