Linked Data
ClinVar Variation Id:
328542
dbSNP Id:
rs45602038
ExAC:
19:17999239 C / T
gnomAD v2:
19-17999239-C-T
gnomAD v3:
19-17888430-C-T
gnomAD v4:
19-17888430-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.17888430C>T , CM000681.2:g.17888430C>T | GRCh38 |
| NC_000019.9:g.17999239C>T , CM000681.1:g.17999239C>T | GRCh37 |
| NC_000019.8:g.17860239C>T | NCBI36 |
| NG_012930.1:g.21458C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222248.4:c.1626C>T MANE Select | ENSP00000222248.2:p.Cys542= | |
| ENST00000222248.3:c.1626C>T | ENSP00000222248.2:p.Cys542= | |
| NM_000453.2:c.1626C>T | NP_000444.1:p.Cys542= | |
| XM_011528192.1:c.1659C>T | XP_011526494.1:p.Cys553= | |
| XM_011528193.1:c.1392C>T | XP_011526495.1:p.Cys464= | |
| XM_011528194.1:c.1293C>T | XP_011526496.1:p.Cys431= | |
| XM_011528192.2:c.1659C>T | XP_011526494.1:p.Cys553= | |
| XM_011528193.3:c.1392C>T | XP_011526495.1:p.Cys464= | |
| XM_011528194.3:c.1293C>T | XP_011526496.1:p.Cys431= | |
| XM_017027158.1:c.1359C>T | XP_016882647.1:p.Cys453= | |
| NM_000453.3:c.1626C>T MANE Select | NP_000444.1:p.Cys542= |