Linked Data
dbSNP Id:
rs746860881
ExAC:
17:72916174 C / A
gnomAD v2:
17-72916174-C-A
gnomAD v4:
17-74920079-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74920079C>A , CM000679.2:g.74920079C>A | GRCh38 |
| NC_000017.10:g.72916174C>A , CM000679.1:g.72916174C>A | GRCh37 |
| NC_000017.9:g.70427769C>A | NCBI36 |
| NG_007882.1:g.8178G>T | |
| NG_033062.1:g.805C>A | |
| NG_007882.2:g.8185G>T | |
| NG_033062.2:g.805C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614341.5:c.757G>T MANE Select | ENSP00000480279.1:p.Val253Leu | |
| ENST00000579243.1:c.*356G>T | ENSP00000462568.1:n.*356G>T | |
| ENST00000614341.4:c.757G>T | ENSP00000480279.1:p.Val253Leu | |
| NM_001282489.2:c.448G>T | NP_001269418.1:p.Val150Leu | |
| NM_173477.4:c.757G>T | NP_775748.2:p.Val253Leu | |
| XM_011524296.1:c.448G>T | XP_011522598.1:p.Val150Leu | |
| XM_011524296.2:c.448G>T | XP_011522598.1:p.Val150Leu | |
| NM_173477.5:c.757G>T MANE Select | NP_775748.2:p.Val253Leu | |
| NM_001282489.3:c.448G>T | NP_001269418.1:p.Val150Leu |