Linked Data
dbSNP Id:
rs374384105
ExAC:
17:39780686 G / A
gnomAD v2:
17-39780686-G-A
gnomAD v3:
17-41624434-G-A
gnomAD v4:
17-41624434-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624434G>A , CM000679.2:g.41624434G>A | GRCh38 |
| NC_000017.10:g.39780686G>A , CM000679.1:g.39780686G>A | GRCh37 |
| NC_000017.9:g.37034212G>A | NCBI36 |
| NG_008625.1:g.5197C>T | |
| NG_009090.2:g.167279C>T , LRG_401:g.167279C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.76C>T MANE Select | ENSP00000308452.8:p.Arg26Cys | |
| ENST00000311208.12:c.76C>T | ENSP00000308452.8:p.Arg26Cys | |
| ENST00000463128.5:c.-312-228C>T | ENSP00000468672.1:n.-312-228C>T | |
| ENST00000491673.1:n.142C>T | ||
| ENST00000540235.5:c.-130C>T | ENSP00000441751.2:n.-130C>T | |
| ENST00000577817.3:c.31C>T | ENSP00000467418.1:p.Arg11Cys | |
| NM_000422.2:c.76C>T | NP_000413.1:p.Arg26Cys | |
| NM_000422.3:c.76C>T MANE Select | NP_000413.1:p.Arg26Cys |