Linked Data
dbSNP Id:
rs1468606669
gnomAD v2:
11-46749706-C-T
gnomAD v4:
11-46728156-C-T
COSMIC:
COSM1638847
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.46728156C>T , CM000673.2:g.46728156C>T | GRCh38 |
| NC_000011.9:g.46749706C>T , CM000673.1:g.46749706C>T | GRCh37 |
| NC_000011.8:g.46706282C>T | NCBI36 |
| NG_008953.1:g.13964C>T , LRG_551:g.13964C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311907.10:c.1291C>T MANE Select | ENSP00000308541.5:p.Arg431Cys | |
| ENST00000311907.9:c.1291C>T | ENSP00000308541.5:p.Arg431Cys | |
| ENST00000530231.5:c.1291C>T | ENSP00000433907.1:p.Arg431Cys | |
| NM_000506.3:c.1291C>T | NP_000497.1:p.Arg431Cys | |
| NM_000506.4:c.1291C>T , LRG_551t1:c.1291C>T | NP_000497.1:p.Arg431Cys | |
| NM_001311257.1:c.1243C>T | NP_001298186.1:p.Arg415Cys | |
| XR_428840.2:n.1335C>T | ||
| XR_428840.4:n.1326C>T | ||
| NM_000506.5:c.1291C>T MANE Select | NP_000497.1:p.Arg431Cys | |
| NM_001311257.2:c.1243C>T | NP_001298186.1:p.Arg415Cys |