Linked Data
ClinVar Variation Id:
1077472
ClinVar RCV Id:
RCV001392050
dbSNP Id:
rs2102661437
MyVariant Identifiers:
chr1:g.215844539G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215671197G>C , CM000663.2:g.215671197G>C | GRCh38 |
| NC_000001.10:g.215844539G>C , CM000663.1:g.215844539G>C | GRCh37 |
| NC_000001.9:g.213911162G>C | NCBI36 |
| NG_009497.1:g.757200C>G | |
| NG_009497.2:g.757252C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.13908C>G MANE Select | ENSP00000305941.3:p.Pro4636= | |
| ENST00000674083.1:c.13908C>G | ENSP00000501296.1:p.Pro4636= | |
| ENST00000307340.7:c.13908C>G | ENSP00000305941.3:p.Pro4636= | |
| NM_206933.2:c.13908C>G | NP_996816.2:p.Pro4636= | |
| NM_206933.3:c.13908C>G | NP_996816.2:p.Pro4636= | |
| NM_206933.4:c.13908C>G MANE Select | NP_996816.3:p.Pro4636= |