Linked Data
ClinVar Variation Id:
438034
ClinVar RCV Id:
RCV000504675
dbSNP Id:
rs1553263639
PubMed:
PMID:28041643
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215799080C>A , CM000663.2:g.215799080C>A | GRCh38 |
| NC_000001.10:g.215972422C>A , CM000663.1:g.215972422C>A | GRCh37 |
| NC_000001.9:g.214039045C>A | NCBI36 |
| NG_009497.1:g.629317G>T | |
| NG_009497.2:g.629369G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.9785G>T MANE Select | ENSP00000305941.3:p.Gly3262Val | |
| ENST00000674083.1:c.9785G>T | ENSP00000501296.1:p.Gly3262Val | |
| ENST00000307340.7:c.9785G>T | ENSP00000305941.3:p.Gly3262Val | |
| NM_206933.2:c.9785G>T | NP_996816.2:p.Gly3262Val | |
| NM_206933.3:c.9785G>T | NP_996816.2:p.Gly3262Val | |
| NM_206933.4:c.9785G>T MANE Select | NP_996816.3:p.Gly3262Val |