Linked Data
dbSNP Id:
rs759922718
gnomAD v2:
7-150036566-A-G
gnomAD v3:
7-150339477-A-G
gnomAD v4:
7-150339477-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150339477A>G , CM000669.2:g.150339477A>G | GRCh38 |
| NC_000007.13:g.150036566A>G , CM000669.1:g.150036566A>G | GRCh37 |
| NC_000007.12:g.149667499A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000223271.8:c.280-396T>C MANE Select | ENSP00000223271.3:n.280-396T>C | |
| ENST00000223271.7:c.280-396T>C | ENSP00000223271.3:n.280-396T>C | |
| ENST00000466675.5:c.280-396T>C | ENSP00000418009.1:n.280-396T>C | |
| ENST00000467793.5:c.280-396T>C | ENSP00000417669.1:n.280-396T>C | |
| ENST00000478771.2:n.1562-396T>C | ||
| ENST00000482669.1:c.280-396T>C | ENSP00000418483.1:n.280-396T>C | |
| NM_002889.3:c.280-396T>C | NP_002880.1:n.280-396T>C | |
| XM_017012491.1:c.280-396T>C | XP_016867980.1:n.280-396T>C | |
| NM_002889.4:c.280-396T>C MANE Select | NP_002880.1:n.280-396T>C |