Linked Data
dbSNP Id:
rs1601791339
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.30304723A>T , CM000685.2:g.30304723A>T | GRCh38 |
| NC_000023.10:g.30322840A>T , CM000685.1:g.30322840A>T | GRCh37 |
| NC_000023.9:g.30232761A>T | NCBI36 |
| NG_009814.1:g.9656T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378970.5:c.1269T>A MANE Select | ENSP00000368253.4:p.His423Gln | |
| ENST00000378970.4:c.1269T>A | ENSP00000368253.4:p.His423Gln | |
| NM_000475.4:c.1269T>A | NP_000466.2:p.His423Gln | |
| NM_000475.5:c.1269T>A MANE Select | NP_000466.2:p.His423Gln |