Linked Data
ClinVar Variation Id:
896820
ClinVar RCV Id:
RCV001139729
dbSNP Id:
rs1692290741
MyVariant Identifiers:
chr2:g.203329653C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202464930C>T , CM000664.2:g.202464930C>T | GRCh38 |
| NC_000002.11:g.203329653C>T , CM000664.1:g.203329653C>T | GRCh37 |
| NC_000002.10:g.203037898C>T | NCBI36 |
| NG_009363.1:g.93604C>T , LRG_712:g.93604C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.198C>T MANE Select | ENSP00000363708.4:p.Cys66= | |
| ENST00000638587.1:c.123C>T | ENSP00000491062.1:p.Cys41= | |
| ENST00000374574.2:c.198C>T | ENSP00000363702.2:p.Cys66= | |
| ENST00000374580.8:c.198C>T | ENSP00000363708.4:p.Cys66= | |
| ENST00000479069.1:n.105C>T | ||
| NM_001204.6:c.198C>T , LRG_712t1:c.198C>T | NP_001195.2:p.Cys66= | |
| XM_011511687.1:c.198C>T | XP_011509989.1:p.Cys66= | |
| XM_011511688.1:c.198C>T | XP_011509990.1:p.Cys66= | |
| NM_001204.7:c.198C>T MANE Select | NP_001195.2:p.Cys66= |