Linked Data
ClinVar Variation Id:
2089542
ClinVar RCV Id:
RCV003005603
MyVariant Identifiers:
chr1:g.215972319G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215798977G>A , CM000663.2:g.215798977G>A | GRCh38 |
| NC_000001.10:g.215972319G>A , CM000663.1:g.215972319G>A | GRCh37 |
| NC_000001.9:g.214038942G>A | NCBI36 |
| NG_009497.1:g.629420C>T | |
| NG_009497.2:g.629472C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307340.8:c.9888C>T MANE Select | ENSP00000305941.3:p.Gly3296= | |
| ENST00000674083.1:c.9888C>T | ENSP00000501296.1:p.Gly3296= | |
| ENST00000307340.7:c.9888C>T | ENSP00000305941.3:p.Gly3296= | |
| NM_206933.2:c.9888C>T | NP_996816.2:p.Gly3296= | |
| NM_206933.3:c.9888C>T | NP_996816.2:p.Gly3296= | |
| NM_206933.4:c.9888C>T MANE Select | NP_996816.3:p.Gly3296= |