Linked Data
dbSNP Id:
rs756260407
gnomAD v2:
22-43559019-G-A
gnomAD v3:
22-43163013-G-A
gnomAD v4:
22-43163013-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43163013G>A , CM000684.2:g.43163013G>A | GRCh38 |
| NC_000022.10:g.43559019G>A , CM000684.1:g.43559019G>A | GRCh37 |
| NC_000022.9:g.41888963G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337554.8:c.*22G>A MANE Select | ENSP00000338004.3:n.*22G>A | |
| ENST00000329563.8:c.*22G>A | ENSP00000328973.4:n.*22G>A | |
| ENST00000337554.7:c.*22G>A | ENSP00000338004.3:n.*22G>A | |
| ENST00000396265.4:c.*22G>A | ENSP00000379563.4:n.*22G>A | |
| ENST00000583777.5:c.*22G>A | ENSP00000463495.1:n.*22G>A | |
| NM_000714.5:c.*22G>A | NP_000705.2:n.*22G>A | |
| NM_001256530.1:c.*22G>A | NP_001243459.1:n.*22G>A | |
| NM_001256531.1:c.*22G>A | NP_001243460.1:n.*22G>A | |
| NR_046308.1:n.441G>A | ||
| NM_000714.6:c.*22G>A MANE Select | NP_000705.2:n.*22G>A | |
| NR_046308.2:n.396G>A |