Linked Data
gnomAD v4:
16-67435980-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67435980G>A , CM000678.2:g.67435980G>A | GRCh38 |
| NC_000016.9:g.67469883G>A , CM000678.1:g.67469883G>A | GRCh37 |
| NC_000016.8:g.66027384G>A | NCBI36 |
| NG_016549.1:g.9848G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326152.6:c.502G>A MANE Select | ENSP00000316786.5:p.Ala168Thr | |
| ENST00000326152.5:c.502G>A | ENSP00000316786.5:p.Ala168Thr | |
| ENST00000566606.1:c.480G>A | ENSP00000473429.1:n.480G>A | |
| ENST00000567684.2:n.365G>A | ||
| NM_000196.3:c.502G>A | NP_000187.3:p.Ala168Thr | |
| NM_000196.4:c.502G>A MANE Select | NP_000187.3:p.Ala168Thr |