Linked Data
dbSNP Id:
rs119469015
ExAC:
21:47570043 C / T
gnomAD v2:
21-47570043-C-T
gnomAD v3:
21-46150129-C-T
gnomAD v4:
21-46150129-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46150129C>T , CM000683.2:g.46150129C>T | GRCh38 |
| NC_000021.8:g.47570043C>T , CM000683.1:g.47570043C>T | GRCh37 |
| NC_000021.7:g.46394471C>T | NCBI36 |
| NG_016191.1:g.10439G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000397746.8:c.896G>A MANE Select | ENSP00000380854.3:p.Arg299Gln | |
| ENST00000291670.9:c.896G>A | ENSP00000291670.5:p.Arg299Gln | |
| ENST00000397743.1:c.896G>A | ENSP00000380851.1:p.Arg299Gln | |
| ENST00000397746.7:c.896G>A | ENSP00000380854.3:p.Arg299Gln | |
| ENST00000397748.5:c.896G>A | ENSP00000380856.1:p.Arg299Gln | |
| ENST00000498355.6:n.965G>A | ||
| NM_006657.2:c.896G>A | NP_006648.1:p.Arg299Gln | |
| NM_206965.1:c.896G>A | NP_996848.1:p.Arg299Gln | |
| XM_006723961.2:c.1016G>A | XP_006724024.2:p.Arg339Gln | |
| XM_006723962.2:c.1016G>A | XP_006724025.2:p.Arg339Gln | |
| XM_011529434.1:c.1016G>A | XP_011527736.1:p.Arg339Gln | |
| XM_011529435.1:c.1016G>A | XP_011527737.1:p.Arg339Gln | |
| XM_011529436.1:c.1016G>A | XP_011527738.1:p.Arg339Gln | |
| XM_011529437.1:c.1016G>A | XP_011527739.1:p.Arg339Gln | |
| XM_011529438.1:c.1016G>A | XP_011527740.1:p.Arg339Gln | |
| XM_011529439.1:c.503G>A | XP_011527741.1:p.Arg168Gln | |
| XM_011529440.1:c.1016G>A | XP_011527742.1:p.Arg339Gln | |
| XR_937433.1:n.1199G>A | ||
| NM_001320412.1:c.896G>A | NP_001307341.1:p.Arg299Gln | |
| XM_006723961.4:c.1016G>A | XP_006724024.2:p.Arg339Gln | |
| XM_006723962.4:c.1016G>A | XP_006724025.2:p.Arg339Gln | |
| XM_011529434.3:c.1016G>A | XP_011527736.1:p.Arg339Gln | |
| XM_011529435.3:c.1016G>A | XP_011527737.1:p.Arg339Gln | |
| XM_011529436.3:c.1016G>A | XP_011527738.1:p.Arg339Gln | |
| XM_011529437.3:c.1016G>A | XP_011527739.1:p.Arg339Gln | |
| XM_011529439.2:c.503G>A | XP_011527741.1:p.Arg168Gln | |
| XM_011529440.3:c.1016G>A | XP_011527742.1:p.Arg339Gln | |
| XR_937433.3:n.1233G>A | ||
| NM_206965.2:c.896G>A MANE Select | NP_996848.1:p.Arg299Gln | |
| NM_001320412.2:c.896G>A | NP_001307341.1:p.Arg299Gln | |
| NM_006657.3:c.896G>A | NP_006648.1:p.Arg299Gln |