Linked Data
ClinVar Variation Id:
2586690
ClinVar RCV Id:
RCV003360692
MyVariant Identifiers:
chr2:g.29443647C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29220781C>A , CM000664.2:g.29220781C>A | GRCh38 |
| NC_000002.11:g.29443647C>A , CM000664.1:g.29443647C>A | GRCh37 |
| NC_000002.10:g.29297151C>A | NCBI36 |
| NG_009445.1:g.705786G>T , LRG_488:g.705786G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.3570G>T MANE Select | ENSP00000373700.3:p.Leu1190= | |
| ENST00000431873.6:c.797G>T | ||
| ENST00000638605.1:n.447G>T | ||
| ENST00000642122.1:c.366G>T | ENSP00000493203.1:p.Leu122= | |
| ENST00000389048.7:c.3570G>T | ENSP00000373700.3:p.Leu1190= | |
| ENST00000431873.5:c.450G>T | ENSP00000414027.2:p.Leu150= | |
| ENST00000618119.4:c.2439G>T | ENSP00000482733.1:p.Leu813= | |
| NM_004304.4:c.3570G>T | NP_004295.2:p.Leu1190= | |
| NM_001353765.1:c.366G>T | NP_001340694.1:p.Leu122= | |
| XM_024452778.1:c.723G>T | XP_024308546.1:p.Leu241= | |
| XM_024452779.1:c.366G>T | XP_024308547.1:p.Leu122= | |
| NM_004304.5:c.3570G>T MANE Select | NP_004295.2:p.Leu1190= | |
| NM_001353765.2:c.366G>T | NP_001340694.1:p.Leu122= |