Linked Data
dbSNP Id:
rs1553602933
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14130817C>A , CM000665.2:g.14130817C>A | GRCh38 |
| NC_000003.11:g.14172317C>A , CM000665.1:g.14172317C>A | GRCh37 |
| NC_000003.10:g.14147318C>A | NCBI36 |
| NG_008975.1:g.10878C>A , LRG_435:g.10878C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432444.2:c.*193-5C>A | ENSP00000395617.1:n.*193-5C>A | |
| ENST00000306077.5:c.163-5C>A MANE Select | ENSP00000303992.5:n.163-5C>A | |
| ENST00000306077.4:c.163-5C>A | ENSP00000303992.4:n.163-5C>A | |
| ENST00000432444.1:c.*193-5C>A | ENSP00000395617.1:n.*193-5C>A | |
| NM_024334.2:c.163-5C>A , LRG_435t1:c.163-5C>A | NP_077310.1:n.163-5C>A | |
| XM_011534109.1:c.58-5C>A | XP_011532411.1:n.58-5C>A | |
| XM_017007176.2:c.58-5C>A | XP_016862665.1:n.58-5C>A | |
| NM_024334.3:c.163-5C>A MANE Select | NP_077310.1:n.163-5C>A |