Linked Data
ClinVar Variation Id:
56517
dbSNP Id:
rs386833955
gnomAD v4:
19-35849655-T-G
PubMed:
PMID:18614772
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35849655T>G , CM000681.2:g.35849655T>G | GRCh38 |
| NC_000019.9:g.36340557T>G , CM000681.1:g.36340557T>G | GRCh37 |
| NC_000019.8:g.41032397T>G | NCBI36 |
| NG_013356.2:g.24633A>C , LRG_693:g.24633A>C | |
| NG_051206.1:g.3021T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378910.10:c.609-2A>C MANE Select | ENSP00000368190.4:n.609-2A>C | |
| ENST00000353632.6:c.609-2A>C | ENSP00000343634.5:n.609-2A>C | |
| ENST00000378910.9:c.609-2A>C | ENSP00000368190.4:n.609-2A>C | |
| NM_004646.3:c.609-2A>C , LRG_693t1:c.609-2A>C | NP_004637.1:n.609-2A>C | |
| NM_004646.4:c.609-2A>C MANE Select | NP_004637.1:n.609-2A>C |