Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.19353170G>T , CM000664.2:g.19353170G>T | GRCh38 |
| NC_000002.11:g.19552931G>T , CM000664.1:g.19552931G>T | GRCh37 |
| NC_000002.10:g.19416412G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272223.3:c.636C>A MANE Select | ENSP00000272223.2:p.Phe212Leu | |
| ENST00000272223.2:c.636C>A | ENSP00000272223.2:p.Phe212Leu | |
| ENST00000487581.1:n.3743C>A | ||
| NM_145260.2:c.636C>A | NP_660303.1:p.Phe212Leu | |
| XM_006711942.2:c.636C>A | XP_006712005.1:p.Phe212Leu | |
| XM_006711942.4:c.636C>A | XP_006712005.1:p.Phe212Leu | |
| NM_145260.3:c.636C>A MANE Select | NP_660303.1:p.Phe212Leu |