Linked Data
ClinVar Variation Id:
3074230
ClinVar RCV Id:
RCV004012772
MyVariant Identifiers:
chr11:g.2594201G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2572971G>C , CM000673.2:g.2572971G>C | GRCh38 |
| NC_000011.9:g.2594201G>C , CM000673.1:g.2594201G>C | GRCh37 |
| NC_000011.8:g.2550777G>C | NCBI36 |
| NG_008935.1:g.132981G>C , LRG_287:g.132981G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.645G>C | ENSP00000434560.2:p.Ala215= | |
| ENST00000646564.2:c.478-10464G>C | ENSP00000495806.2:n.478-10464G>C | |
| ENST00000155840.12:c.906G>C MANE Select | ENSP00000155840.2:p.Ala302= | |
| ENST00000335475.6:c.525G>C | ENSP00000334497.5:p.Ala175= | |
| ENST00000646564.1:c.124-10464G>C | ENSP00000495806.1:n.124-10464G>C | |
| ENST00000155840.9:c.906G>C | ENSP00000155840.2:p.Ala302= | |
| ENST00000335475.5:c.525G>C | ENSP00000334497.5:p.Ala175= | |
| NM_000218.2:c.906G>C , LRG_287t1:c.906G>C | NP_000209.2:p.Ala302= | |
| NM_181798.1:c.525G>C , LRG_287t2:c.525G>C | NP_861463.1:p.Ala175= | |
| NM_000218.3:c.906G>C MANE Select | NP_000209.2:p.Ala302= |