Linked Data
dbSNP Id:
rs781272193
ExAC:
8:100874086 C / A
gnomAD v2:
8-100874086-C-A
gnomAD v4:
8-99861858-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.99861858C>A , CM000670.2:g.99861858C>A | GRCh38 |
| NC_000008.10:g.100874086C>A , CM000670.1:g.100874086C>A | GRCh37 |
| NC_000008.9:g.100943262C>A | NCBI36 |
| NG_007098.2:g.853593C>A , LRG_351:g.853593C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682153.1:c.*296C>A | ENSP00000507923.1:n.*296C>A | |
| ENST00000682358.1:n.11272C>A | ||
| ENST00000683334.1:c.*6884C>A | ENSP00000507369.1:n.*6884C>A | |
| ENST00000357162.7:c.11127C>A MANE Select | ENSP00000349685.2:p.Asn3709Lys | |
| ENST00000358544.7:c.11202C>A MANE Plus Clinical | ENSP00000351346.2:p.Asn3734Lys | |
| ENST00000357162.6:c.11127C>A | ENSP00000349685.2:p.Asn3709Lys | |
| ENST00000358544.6:c.11202C>A | ENSP00000351346.2:p.Asn3734Lys | |
| NM_017890.4:c.11202C>A , LRG_351t1:c.11202C>A | NP_060360.3:p.Asn3734Lys | |
| NM_152564.4:c.11127C>A , LRG_351t2:c.11127C>A | NP_689777.3:p.Asn3709Lys | |
| XM_005250800.2:c.11202C>A | XP_005250857.1:p.Asn3734Lys | |
| XM_005250801.3:c.11202C>A | XP_005250858.1:p.Asn3734Lys | |
| XM_011516848.1:c.11199C>A | XP_011515150.1:p.Asn3733Lys | |
| XM_011516849.1:c.11124C>A | XP_011515151.1:p.Asn3708Lys | |
| XM_011516850.1:c.10824C>A | XP_011515152.1:p.Asn3608Lys | |
| XM_011516851.1:c.8088C>A | XP_011515153.1:p.Asn2696Lys | |
| XM_011516852.1:c.8088C>A | XP_011515154.1:p.Asn2696Lys | |
| XM_011516854.1:c.6981C>A | XP_011515156.1:p.Asn2327Lys | |
| XM_005250800.3:c.11202C>A | XP_005250857.1:p.Asn3734Lys | |
| XM_005250801.5:c.11202C>A | XP_005250858.1:p.Asn3734Lys | |
| XM_011516848.2:c.11199C>A | XP_011515150.1:p.Asn3733Lys | |
| XM_011516849.2:c.11124C>A | XP_011515151.1:p.Asn3708Lys | |
| XM_011516850.2:c.10824C>A | XP_011515152.1:p.Asn3608Lys | |
| XM_011516851.2:c.8088C>A | XP_011515153.1:p.Asn2696Lys | |
| XM_011516852.2:c.8088C>A | XP_011515154.1:p.Asn2696Lys | |
| XM_011516854.2:c.6981C>A | XP_011515156.1:p.Asn2327Lys | |
| XM_017013109.1:c.11007C>A | XP_016868598.1:p.Asn3669Lys | |
| XM_017013111.1:c.8088C>A | XP_016868600.1:p.Asn2696Lys | |
| XM_017013112.1:c.6759C>A | XP_016868601.1:p.Asn2253Lys | |
| XM_024447074.1:c.9987C>A | XP_024302842.1:p.Asn3329Lys | |
| NM_017890.5:c.11202C>A MANE Plus Clinical | NP_060360.3:p.Asn3734Lys | |
| NM_152564.5:c.11127C>A MANE Select | NP_689777.3:p.Asn3709Lys |