Linked Data
gnomAD v4:
17-74919895-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74919895G>T , CM000679.2:g.74919895G>T | GRCh38 |
| NC_000017.10:g.72915990G>T , CM000679.1:g.72915990G>T | GRCh37 |
| NC_000017.9:g.70427585G>T | NCBI36 |
| NG_007882.1:g.8362C>A | |
| NG_033062.1:g.621G>T | |
| NG_007882.2:g.8369C>A | |
| NG_033062.2:g.621G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000614341.5:c.941C>A MANE Select | ENSP00000480279.1:p.Thr314Asn | |
| ENST00000579243.1:c.*540C>A | ENSP00000462568.1:n.*540C>A | |
| ENST00000614341.4:c.941C>A | ENSP00000480279.1:p.Thr314Asn | |
| NM_001282489.2:c.632C>A | NP_001269418.1:p.Thr211Asn | |
| NM_173477.4:c.941C>A | NP_775748.2:p.Thr314Asn | |
| XM_011524296.1:c.632C>A | XP_011522598.1:p.Thr211Asn | |
| XM_011524296.2:c.632C>A | XP_011522598.1:p.Thr211Asn | |
| NM_173477.5:c.941C>A MANE Select | NP_775748.2:p.Thr314Asn | |
| NM_001282489.3:c.632C>A | NP_001269418.1:p.Thr211Asn |