Linked Data
ClinVar Variation Id:
1145920
ClinVar RCV Id:
RCV001484972
dbSNP Id:
rs2113699646
MyVariant Identifiers:
chr5:g.149361205G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149981642G>T , CM000667.2:g.149981642G>T | GRCh38 |
| NC_000005.9:g.149361205G>T , CM000667.1:g.149361205G>T | GRCh37 |
| NC_000005.8:g.149341398G>T | NCBI36 |
| NG_007147.2:g.22760G>T , LRG_684:g.22760G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286298.5:c.2049G>T MANE Select | ENSP00000286298.4:p.Leu683= | |
| ENST00000286298.4:c.2049G>T | ENSP00000286298.4:p.Leu683= | |
| ENST00000503336.1:c.372+3291G>T | ENSP00000426053.1:n.372+3291G>T | |
| NM_000112.3:c.2049G>T , LRG_684t1:c.2049G>T | NP_000103.2:p.Leu683= | |
| XM_017009191.2:c.2049G>T | XP_016864680.1:p.Leu683= | |
| NM_000112.4:c.2049G>T MANE Select | NP_000103.2:p.Leu683= |