Linked Data
dbSNP Id:
rs1401588470
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272632C>A , CM000676.2:g.91272632C>A | GRCh38 |
| NC_000014.8:g.91738976C>A , CM000676.1:g.91738976C>A | GRCh37 |
| NC_000014.7:g.90808729C>A | NCBI36 |
| NG_033118.1:g.150213G>T | |
| NG_033118.2:g.150213G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.6080G>T MANE Select | ENSP00000374507.6:p.Cys2027Phe | |
| ENST00000331194.8:c.1514G>T | ENSP00000330332.8:p.Cys505Phe | |
| ENST00000389857.10:c.6080G>T | ENSP00000374507.6:p.Cys2027Phe | |
| ENST00000556726.5:c.2308G>T | ||
| NM_001080414.3:c.6080G>T | NP_001073883.2:p.Cys2027Phe | |
| XM_011536796.1:c.5972G>T | XP_011535098.1:p.Cys1991Phe | |
| XM_011536796.2:c.5972G>T | XP_011535098.1:p.Cys1991Phe | |
| XM_017021336.1:c.3161G>T | XP_016876825.1:p.Cys1054Phe | |
| NM_001080414.4:c.6080G>T MANE Select | NP_001073883.2:p.Cys2027Phe |