Linked Data
ClinVar Variation Id:
1156167
ClinVar RCV Id:
RCV001498713
dbSNP Id:
rs2102545801
MyVariant Identifiers:
chr1:g.216420297C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.216246955C>G , CM000663.2:g.216246955C>G | GRCh38 |
| NC_000001.10:g.216420297C>G , CM000663.1:g.216420297C>G | GRCh37 |
| NC_000001.9:g.214486920C>G | NCBI36 |
| NG_009497.1:g.181442G>C | |
| NG_009497.2:g.181494G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.2439G>C MANE Select | ENSP00000305941.3:p.Gly813= | |
| ENST00000674083.1:c.2439G>C | ENSP00000501296.1:p.Gly813= | |
| ENST00000307340.7:c.2439G>C | ENSP00000305941.3:p.Gly813= | |
| ENST00000366942.3:c.2439G>C | ENSP00000355909.3:p.Gly813= | |
| NM_007123.5:c.2439G>C | NP_009054.5:p.Gly813= | |
| NM_206933.2:c.2439G>C | NP_996816.2:p.Gly813= | |
| NM_206933.3:c.2439G>C | NP_996816.2:p.Gly813= | |
| NM_007123.6:c.2439G>C | NP_009054.6:p.Gly813= | |
| NM_206933.4:c.2439G>C MANE Select | NP_996816.3:p.Gly813= |