Linked Data
dbSNP Id:
rs1891226315
gnomAD v4:
15-28141561-C-T
MyVariant Identifiers:
chr15:g.28386707C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.28141561C>T , CM000677.2:g.28141561C>T | GRCh38 |
| NC_000015.9:g.28386707C>T , CM000677.1:g.28386707C>T | GRCh37 |
| NC_000015.8:g.26060302C>T | NCBI36 |
| NG_016355.1:g.185589G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261609.13:c.11886G>A MANE Select | ENSP00000261609.8:p.Arg3962= | |
| ENST00000650509.1:c.3597G>A | ENSP00000496936.1:p.Arg1199= | |
| ENST00000261609.11:c.11886G>A | ENSP00000261609.7:p.Arg3962= | |
| NM_004667.5:c.11886G>A | NP_004658.3:p.Arg3962= | |
| XM_005268276.3:c.11772G>A | XP_005268333.1:p.Arg3924= | |
| XM_005268277.3:c.11772G>A | XP_005268334.1:p.Arg3924= | |
| XM_006720726.2:c.11871G>A | XP_006720789.1:p.Arg3957= | |
| XM_006720727.2:c.11628G>A | XP_006720790.1:p.Arg3876= | |
| XM_011522131.1:c.11403G>A | XP_011520433.1:p.Arg3801= | |
| XM_011522132.1:c.9402G>A | XP_011520434.1:p.Arg3134= | |
| XM_011522133.1:c.8631G>A | XP_011520435.1:p.Arg2877= | |
| XM_011522134.1:c.6003G>A | XP_011520436.1:p.Arg2001= | |
| XM_005268276.5:c.11772G>A | XP_005268333.1:p.Arg3924= | |
| XM_006720726.3:c.11871G>A | XP_006720789.1:p.Arg3957= | |
| XM_006720727.3:c.11628G>A | XP_006720790.1:p.Arg3876= | |
| XM_017022695.1:c.11772G>A | XP_016878184.1:p.Arg3924= | |
| XM_017022696.1:c.11772G>A | XP_016878185.1:p.Arg3924= | |
| XM_017022697.1:c.5052G>A | XP_016878186.1:p.Arg1684= | |
| XM_017022698.1:c.5052G>A | XP_016878187.1:p.Arg1684= | |
| NM_004667.6:c.11886G>A MANE Select | NP_004658.3:p.Arg3962= |