Linked Data
ClinVar Variation Id:
1756782
ClinVar RCV Id:
RCV002364924
gnomAD v4:
11-2572031-G-A
MyVariant Identifiers:
chr11:g.2593261G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2572031G>A , CM000673.2:g.2572031G>A | GRCh38 |
| NC_000011.9:g.2593261G>A , CM000673.1:g.2593261G>A | GRCh37 |
| NC_000011.8:g.2549837G>A | NCBI36 |
| NG_008935.1:g.132041G>A , LRG_287:g.132041G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.441G>A | ENSP00000434560.2:p.Gln147= | |
| ENST00000646564.2:c.478-11404G>A | ENSP00000495806.2:n.478-11404G>A | |
| ENST00000155840.12:c.702G>A MANE Select | ENSP00000155840.2:p.Gln234= | |
| ENST00000335475.6:c.321G>A | ENSP00000334497.5:p.Gln107= | |
| ENST00000646564.1:c.124-11404G>A | ENSP00000495806.1:n.124-11404G>A | |
| ENST00000155840.9:c.702G>A | ENSP00000155840.2:p.Gln234= | |
| ENST00000335475.5:c.321G>A | ENSP00000334497.5:p.Gln107= | |
| ENST00000496887.6:c.441G>A | ENSP00000434560.1:p.Gln147= | |
| NM_000218.2:c.702G>A , LRG_287t1:c.702G>A | NP_000209.2:p.Gln234= | |
| NM_181798.1:c.321G>A , LRG_287t2:c.321G>A | NP_861463.1:p.Gln107= | |
| NM_000218.3:c.702G>A MANE Select | NP_000209.2:p.Gln234= |