Linked Data
dbSNP Id:
rs770829928
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.23191786G>T , CM000670.2:g.23191786G>T | GRCh38 |
| NC_000008.10:g.23049299G>T , CM000670.1:g.23049299G>T | GRCh37 |
| NC_000008.9:g.23105244G>T | NCBI36 |
| NG_032107.1:g.38382C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221132.8:c.1315C>A MANE Select | ENSP00000221132.3:p.His439Asn | |
| ENST00000221132.7:c.1315C>A | ENSP00000221132.3:p.His439Asn | |
| ENST00000613472.1:c.841C>A | ENSP00000480778.1:p.His281Asn | |
| NM_003844.3:c.1315C>A | NP_003835.3:p.His439Asn | |
| NM_003844.4:c.1315C>A MANE Select | NP_003835.3:p.His439Asn |