Linked Data
ClinVar Variation Id:
1665369
ClinVar RCV Id:
RCV002184099
dbSNP Id:
rs1657986831
MyVariant Identifiers:
chr1:g.215848707A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215675365A>G , CM000663.2:g.215675365A>G | GRCh38 |
| NC_000001.10:g.215848707A>G , CM000663.1:g.215848707A>G | GRCh37 |
| NC_000001.9:g.213915330A>G | NCBI36 |
| NG_009497.1:g.753032T>C | |
| NG_009497.2:g.753084T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.12546T>C MANE Select | ENSP00000305941.3:p.Asn4182= | |
| ENST00000674083.1:c.12546T>C | ENSP00000501296.1:p.Asn4182= | |
| ENST00000307340.7:c.12546T>C | ENSP00000305941.3:p.Asn4182= | |
| NM_206933.2:c.12546T>C | NP_996816.2:p.Asn4182= | |
| NM_206933.3:c.12546T>C | NP_996816.2:p.Asn4182= | |
| NM_206933.4:c.12546T>C MANE Select | NP_996816.3:p.Asn4182= |