Linked Data
ClinVar Variation Id:
188738
dbSNP Id:
rs180177227
gnomAD v2:
2-241810823-G-T
gnomAD v3:
2-240871406-G-T
gnomAD v4:
2-240871406-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240871406G>T , CM000664.2:g.240871406G>T | GRCh38 |
| NC_000002.11:g.241810823G>T , CM000664.1:g.241810823G>T | GRCh37 |
| NC_000002.10:g.241459496G>T | NCBI36 |
| NG_008005.1:g.7662G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.481G>T MANE Select | ENSP00000302620.3:p.Gly161Cys | |
| ENST00000307503.3:c.481G>T | ENSP00000302620.3:p.Gly161Cys | |
| ENST00000472436.1:n.501G>T | ||
| ENST00000476698.1:n.218G>T | ||
| NM_000030.2:c.481G>T | NP_000021.1:p.Gly161Cys | |
| NM_000030.3:c.481G>T MANE Select | NP_000021.1:p.Gly161Cys |