Linked Data
ClinVar Variation Id:
204097
dbSNP Id:
rs180177210
ExAC:
2:241810066 C / T
gnomAD v2:
2-241810066-C-T
gnomAD v4:
2-240870649-C-T
PubMed:
PMID:19479957
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240870649C>T , CM000664.2:g.240870649C>T | GRCh38 |
| NC_000002.11:g.241810066C>T , CM000664.1:g.241810066C>T | GRCh37 |
| NC_000002.10:g.241458739C>T | NCBI36 |
| NG_008005.1:g.6905C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.364C>T MANE Select | ENSP00000302620.3:p.Arg122Ter | |
| ENST00000307503.3:c.364C>T | ENSP00000302620.3:p.Arg122Ter | |
| ENST00000472436.1:n.384C>T | ||
| NM_000030.2:c.364C>T | NP_000021.1:p.Arg122Ter | |
| NM_000030.3:c.364C>T MANE Select | NP_000021.1:p.Arg122Ter |