Linked Data
gnomAD v4:
22-43163217-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43163217C>A , CM000684.2:g.43163217C>A | GRCh38 |
| NC_000022.10:g.43559223C>A , CM000684.1:g.43559223C>A | GRCh37 |
| NC_000022.9:g.41889167C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337554.8:c.*226C>A MANE Select | ENSP00000338004.3:n.*226C>A | |
| ENST00000337554.7:c.*226C>A | ENSP00000338004.3:n.*226C>A | |
| ENST00000396265.4:c.*226C>A | ENSP00000379563.4:n.*226C>A | |
| ENST00000583777.5:c.*226C>A | ENSP00000463495.1:n.*226C>A | |
| NM_000714.5:c.*226C>A | NP_000705.2:n.*226C>A | |
| NM_001256530.1:c.*226C>A | NP_001243459.1:n.*226C>A | |
| NM_001256531.1:c.*226C>A | NP_001243460.1:n.*226C>A | |
| NR_046308.1:n.645C>A | ||
| NM_000714.6:c.*226C>A MANE Select | NP_000705.2:n.*226C>A | |
| NR_046308.2:n.600C>A |