Linked Data
ClinVar Variation Id:
2743995
ClinVar RCV Id:
RCV003560626
MyVariant Identifiers:
chr1:g.215990498A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215817156A>G , CM000663.2:g.215817156A>G | GRCh38 |
| NC_000001.10:g.215990498A>G , CM000663.1:g.215990498A>G | GRCh37 |
| NC_000001.9:g.214057121A>G | NCBI36 |
| NG_009497.1:g.611241T>C | |
| NG_009497.2:g.611293T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.9411T>C MANE Select | ENSP00000305941.3:p.Asn3137= | |
| ENST00000674083.1:c.9411T>C | ENSP00000501296.1:p.Asn3137= | |
| ENST00000307340.7:c.9411T>C | ENSP00000305941.3:p.Asn3137= | |
| NM_206933.2:c.9411T>C | NP_996816.2:p.Asn3137= | |
| NM_206933.3:c.9411T>C | NP_996816.2:p.Asn3137= | |
| NM_206933.4:c.9411T>C MANE Select | NP_996816.3:p.Asn3137= |