Linked Data
dbSNP Id:
rs1255186631
gnomAD v2:
2-169801145-T-A
gnomAD v3:
2-168944635-T-A
gnomAD v4:
2-168944635-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.168944635T>A , CM000664.2:g.168944635T>A | GRCh38 |
| NC_000002.11:g.169801145T>A , CM000664.1:g.169801145T>A | GRCh37 |
| NC_000002.10:g.169509391T>A | NCBI36 |
| NG_007374.1:g.91689A>T | |
| NG_007374.2:g.91762A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649448.1:c.897A>T | ENSP00000497165.1:p.Arg299Ser | |
| ENST00000650372.1:c.2580A>T MANE Select | ENSP00000497931.1:p.Arg860Ser | |
| ENST00000263817.6:c.2580A>T | ENSP00000263817.6:p.Arg860Ser | |
| ENST00000439188.1:c.1269A>T | ENSP00000416058.1:n.1269A>T | |
| NM_003742.2:c.2580A>T | NP_003733.2:p.Arg860Ser | |
| XM_006712817.2:c.2622A>T | XP_006712880.1:p.Arg874Ser | |
| XM_011512077.1:c.2682A>T | XP_011510379.1:p.Arg894Ser | |
| XM_011512078.1:c.2682A>T | XP_011510380.1:p.Arg894Ser | |
| XM_011512079.1:c.2682A>T | XP_011510381.1:p.Arg894Ser | |
| XM_011512080.1:c.2682A>T | XP_011510382.1:p.Arg894Ser | |
| XM_011512081.1:c.906A>T | XP_011510383.1:p.Arg302Ser | |
| NM_003742.4:c.2580A>T MANE Select | NP_003733.2:p.Arg860Ser | |
| XM_006712817.3:c.2622A>T | XP_006712880.1:p.Arg874Ser | |
| XM_011512077.2:c.2682A>T | XP_011510379.1:p.Arg894Ser | |
| XM_011512078.2:c.2682A>T | XP_011510380.1:p.Arg894Ser | |
| XM_011512080.2:c.2682A>T | XP_011510382.1:p.Arg894Ser | |
| XM_011512081.2:c.906A>T | XP_011510383.1:p.Arg302Ser | |
| XM_017005165.1:c.2682A>T | XP_016860654.1:p.Arg894Ser | |
| XM_017005166.1:c.1911A>T | XP_016860655.1:p.Arg637Ser | |
| XM_017005167.1:c.1365A>T | XP_016860656.1:p.Arg455Ser |