Linked Data
gnomAD v4:
16-74713487-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.74713487C>A , CM000678.2:g.74713487C>A | GRCh38 |
| NC_000016.9:g.74747385C>A , CM000678.1:g.74747385C>A | GRCh37 |
| NC_000016.8:g.73304886C>A | NCBI36 |
| NG_017070.1:g.66345G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000219368.8:c.*703G>T MANE Select | ENSP00000219368.3:n.*703G>T | |
| ENST00000219368.7:c.*703G>T | ENSP00000219368.3:n.*703G>T | |
| ENST00000562145.1:n.1543G>T | ||
| NM_024306.4:c.*703G>T | NP_077282.3:n.*703G>T | |
| XM_011523319.1:c.*703G>T | XP_011521621.1:n.*703G>T | |
| XM_011523319.2:c.*703G>T | XP_011521621.1:n.*703G>T | |
| NM_024306.5:c.*703G>T MANE Select | NP_077282.3:n.*703G>T |