Linked Data
ClinVar Variation Id:
1591335
ClinVar RCV Id:
RCV002254769
dbSNP Id:
rs2136511657
MyVariant Identifiers:
chr12:g.56397725A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56003941A>G , CM000674.2:g.56003941A>G | GRCh38 |
| NC_000012.11:g.56397725A>G , CM000674.1:g.56397725A>G | GRCh37 |
| NC_000012.10:g.54683992A>G | NCBI36 |
| NG_008136.1:g.11683A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000266971.8:c.552A>G MANE Select | ENSP00000266971.3:p.Pro184= | |
| ENST00000266971.7:c.552A>G | ENSP00000266971.3:p.Pro184= | |
| ENST00000356124.8:c.552A>G | ENSP00000348440.4:p.Pro184= | |
| ENST00000394109.7:c.552A>G | ENSP00000377668.3:p.Pro184= | |
| ENST00000394115.6:c.552A>G | ENSP00000377674.2:p.Pro184= | |
| ENST00000548274.5:c.552A>G | ENSP00000450245.1:p.Pro184= | |
| ENST00000550065.1:c.552A>G | ENSP00000450264.1:p.Pro184= | |
| ENST00000550340.5:n.437A>G | ||
| ENST00000551698.5:n.574A>G | ||
| ENST00000551841.6:c.268-213A>G | ENSP00000449443.1:n.268-213A>G | |
| NM_000456.2:c.552A>G | NP_000447.2:p.Pro184= | |
| NM_001032386.1:c.552A>G | NP_001027558.1:p.Pro184= | |
| NM_001032387.1:c.552A>G | NP_001027559.1:p.Pro184= | |
| XM_005269112.1:c.573A>G | XP_005269169.1:p.Pro191= | |
| XM_017019905.2:c.573A>G | XP_016875394.1:p.Pro191= | |
| XM_017019906.1:c.573A>G | XP_016875395.1:p.Pro191= | |
| XM_017019907.2:c.552A>G | XP_016875396.1:p.Pro184= | |
| XM_017019908.1:c.552A>G | XP_016875397.1:p.Pro184= | |
| XM_024449167.1:c.573A>G | XP_024304935.1:p.Pro191= | |
| NM_001032386.2:c.552A>G MANE Select | NP_001027558.1:p.Pro184= | |
| NM_000456.3:c.552A>G | NP_000447.2:p.Pro184= | |
| NM_001032387.2:c.552A>G | NP_001027559.1:p.Pro184= |