Linked Data
dbSNP Id:
rs936339807
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31524769G>A , CM000680.2:g.31524769G>A | GRCh38 |
| NC_000018.9:g.29104732G>A , CM000680.1:g.29104732G>A | GRCh37 |
| NC_000018.8:g.27358730G>A | NCBI36 |
| NG_007072.3:g.31528G>A , LRG_397:g.31528G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000682087.2:n.726G>A | ||
| ENST00000683614.2:n.726G>A | ||
| ENST00000682087.1:c.726G>A | ||
| ENST00000683614.1:c.726G>A | ||
| ENST00000261590.13:c.895G>A MANE Select | ENSP00000261590.8:p.Asp299Asn | |
| ENST00000261590.12:c.895G>A | ENSP00000261590.8:p.Asp299Asn | |
| NM_001943.3:c.895G>A , LRG_397t1:c.895G>A | NP_001934.2:p.Asp299Asn | |
| NM_001943.4:c.895G>A | NP_001934.2:p.Asp299Asn | |
| XM_024451095.1:c.361G>A | XP_024306863.1:p.Asp121Asn | |
| NM_001943.5:c.895G>A MANE Select | NP_001934.2:p.Asp299Asn |