Linked Data
dbSNP Id:
rs757977053
ExAC:
19:7117101 C / T
gnomAD v2:
19-7117101-C-T
gnomAD v3:
19-7117090-C-T
gnomAD v4:
19-7117090-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7117090C>T , CM000681.2:g.7117090C>T | GRCh38 |
| NC_000019.9:g.7117101C>T , CM000681.1:g.7117101C>T | GRCh37 |
| NC_000019.8:g.7068101C>T | NCBI36 |
| NG_008852.2:g.181911G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302850.10:c.4115G>A MANE Select | ENSP00000303830.4:p.Arg1372Gln | |
| ENST00000302850.9:c.4115G>A | ENSP00000303830.4:p.Arg1372Gln | |
| ENST00000341500.9:c.4079G>A | ENSP00000342838.4:p.Arg1360Gln | |
| NM_000208.2:c.4115G>A | NP_000199.2:p.Arg1372Gln | |
| NM_000208.3:c.4115G>A | NP_000199.2:p.Arg1372Gln | |
| NM_001079817.1:c.4079G>A | NP_001073285.1:p.Arg1360Gln | |
| NM_001079817.2:c.4079G>A | NP_001073285.1:p.Arg1360Gln | |
| XM_011527988.1:c.4190G>A | XP_011526290.1:p.Arg1397Gln | |
| XM_011527989.1:c.4154G>A | XP_011526291.1:p.Arg1385Gln | |
| XM_011527988.2:c.4112G>A | XP_011526290.2:p.Arg1371Gln | |
| XM_011527989.3:c.4076G>A | XP_011526291.2:p.Arg1359Gln | |
| NM_000208.4:c.4115G>A MANE Select | NP_000199.2:p.Arg1372Gln | |
| NM_001079817.3:c.4079G>A | NP_001073285.1:p.Arg1360Gln |