Linked Data
MyVariant Identifiers:
chr1:g.149897753G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149925861G>A , CM000663.2:g.149925861G>A | GRCh38 |
| NC_000001.10:g.149897753G>A , CM000663.1:g.149897753G>A | GRCh37 |
| NC_000001.9:g.148164377G>A | NCBI36 |
| NG_032777.1:g.7392C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.9:c.888C>T MANE Select | ENSP00000271628.8:p.Phe296= | |
| ENST00000271628.8:c.888C>T | ENSP00000271628.8:p.Phe296= | |
| NM_005850.4:c.888C>T | NP_005841.1:p.Phe296= | |
| NM_005850.5:c.888C>T MANE Select | NP_005841.1:p.Phe296= |