Linked Data
ClinVar Variation Id:
284361
dbSNP Id:
rs141386201
gnomAD v2:
2-44059001-G-A
gnomAD v3:
2-43831862-G-A
gnomAD v4:
2-43831862-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43831862G>A , CM000664.2:g.43831862G>A | GRCh38 |
| NC_000002.11:g.44059001G>A , CM000664.1:g.44059001G>A | GRCh37 |
| NC_000002.10:g.43912505G>A | NCBI36 |
| NG_008883.1:g.11958C>T | |
| NG_008884.2:g.4921G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000405322.8:c.408C>T (ABCG5) MANE Select | ENSP00000384513.2:p.Asp136= | |
| ENST00000644754.1:n.1062C>T (ABCG5) | ||
| ENST00000260645.5:c.408C>T (ABCG5) | ENSP00000260645.1:p.Asp136= | |
| ENST00000405322.5:c.165C>T (ABCG5) | ENSP00000384513.1:p.Asp55= | |
| ENST00000409962.1:c.165C>T (ABCG5) | ENSP00000386501.1:p.Asp55= | |
| ENST00000486512.5:c.165C>T (ABCG5) | ENSP00000430935.1:p.Asp55= | |
| NM_022436.2:c.408C>T (ABCG5) | NP_071881.1:p.Asp136= | |
| XM_005264480.2:c.408C>T (ABCG5) | XP_005264537.1:p.Asp136= | |
| XM_006712073.2:c.408C>T (ABCG5) | XP_006712136.1:p.Asp136= | |
| XM_006712074.2:c.408C>T (ABCG5) | XP_006712137.1:p.Asp136= | |
| XM_011533024.1:c.408C>T (ABCG5) | XP_011531326.1:p.Asp136= | |
| XM_011533025.1:c.165C>T (ABCG5) | XP_011531327.1:p.Asp55= | |
| XM_011533026.1:c.408C>T (ABCG5) | XP_011531328.1:p.Asp136= | |
| XM_011533027.1:c.-12-3747C>T (ABCG5) | XP_011531329.1:n.-12-3747C>T | |
| XM_011533031.1:c.-154+1066G>A (ABCG8) | XP_011531333.1:n.-154+1066G>A | |
| XM_005264480.4:c.408C>T (ABCG5) | XP_005264537.1:p.Asp136= | |
| XM_006712073.3:c.408C>T (ABCG5) | XP_006712136.1:p.Asp136= | |
| XM_006712074.3:c.408C>T (ABCG5) | XP_006712137.1:p.Asp136= | |
| XM_011533024.2:c.408C>T (ABCG5) | XP_011531326.1:p.Asp136= | |
| XM_011533025.3:c.165C>T (ABCG5) | XP_011531327.1:p.Asp55= | |
| XM_011533026.2:c.408C>T (ABCG5) | XP_011531328.1:p.Asp136= | |
| XM_011533027.3:c.-12-3747C>T (ABCG5) | XP_011531329.1:n.-12-3747C>T | |
| NM_022436.3:c.408C>T (ABCG5) MANE Select | NP_071881.1:p.Asp136= |