Linked Data
gnomAD v4:
16-74774412-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.74774412T>C , CM000678.2:g.74774412T>C | GRCh38 |
| NC_000016.9:g.74808310T>C , CM000678.1:g.74808310T>C | GRCh37 |
| NC_000016.8:g.73365811T>C | NCBI36 |
| NG_017070.1:g.5420A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000219368.8:c.270+74A>G MANE Select | ENSP00000219368.3:n.270+74A>G | |
| ENST00000219368.7:c.270+74A>G | ENSP00000219368.3:n.270+74A>G | |
| ENST00000567683.5:c.270+74A>G | ENSP00000455126.1:n.270+74A>G | |
| NM_024306.4:c.270+74A>G | NP_077282.3:n.270+74A>G | |
| XM_011523317.1:c.270+74A>G | XP_011521619.1:n.270+74A>G | |
| XM_011523318.1:c.270+74A>G | XP_011521620.1:n.270+74A>G | |
| XM_011523317.3:c.270+74A>G | XP_011521619.1:n.270+74A>G | |
| NM_024306.5:c.270+74A>G MANE Select | NP_077282.3:n.270+74A>G |