Linked Data
ClinVar Variation Id:
836967
ClinVar RCV Id:
RCV001038203
dbSNP Id:
rs1334812851
MyVariant Identifiers:
chr5:g.149274803G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149895240G>C , CM000667.2:g.149895240G>C | GRCh38 |
| NC_000005.9:g.149274803G>C , CM000667.1:g.149274803G>C | GRCh37 |
| NC_000005.8:g.149254996G>C | NCBI36 |
| NG_009102.1:g.54554C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000255266.10:c.1671C>G MANE Select | ENSP00000255266.5:p.Thr557= | |
| ENST00000255266.9:c.1671C>G | ENSP00000255266.5:p.Thr557= | |
| ENST00000508173.5:n.1855C>G | ||
| ENST00000613228.1:c.1428C>G | ENSP00000478060.1:p.Thr476= | |
| ENST00000617647.4:c.1428C>G | ENSP00000482774.1:p.Thr476= | |
| NM_000440.2:c.1671C>G | NP_000431.2:p.Thr557= | |
| XM_011537648.1:c.1671C>G | XP_011535950.1:p.Thr557= | |
| XM_011537649.1:c.1125C>G | XP_011535951.1:p.Thr375= | |
| XM_011537650.1:c.786C>G | XP_011535952.1:p.Thr262= | |
| XM_011537651.1:c.624C>G | XP_011535953.1:p.Thr208= | |
| XM_011537652.1:c.594C>G | XP_011535954.1:p.Thr198= | |
| XM_011537653.1:c.594C>G | XP_011535955.1:p.Thr198= | |
| XM_011537654.1:c.594C>G | XP_011535956.1:p.Thr198= | |
| XM_011537650.2:c.786C>G | XP_011535952.1:p.Thr262= | |
| XM_011537651.2:c.624C>G | XP_011535953.1:p.Thr208= | |
| XM_011537653.2:c.594C>G | XP_011535955.1:p.Thr198= | |
| XM_011537654.2:c.594C>G | XP_011535956.1:p.Thr198= | |
| XM_017009572.2:c.1428C>G | XP_016865061.1:p.Thr476= | |
| NM_000440.3:c.1671C>G MANE Select | NP_000431.2:p.Thr557= |