Linked Data
dbSNP Id:
rs1300248845
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41623907G>A , CM000679.2:g.41623907G>A | GRCh38 |
| NC_000017.10:g.39780159G>A , CM000679.1:g.39780159G>A | GRCh37 |
| NC_000017.9:g.37033685G>A | NCBI36 |
| NG_008625.1:g.5724C>T | |
| NG_009090.2:g.167806C>T , LRG_401:g.167806C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.432+171C>T MANE Select | ENSP00000308452.8:n.432+171C>T | |
| ENST00000311208.12:c.432+171C>T | ENSP00000308452.8:n.432+171C>T | |
| ENST00000463128.5:c.-184+171C>T | ENSP00000468672.1:n.-184+171C>T | |
| ENST00000491673.1:n.498+171C>T | ||
| ENST00000493253.5:n.219+171C>T | ||
| ENST00000540235.5:c.183+171C>T | ENSP00000441751.2:n.183+171C>T | |
| ENST00000577817.3:c.387+171C>T | ENSP00000467418.1:n.387+171C>T | |
| NM_000422.2:c.432+171C>T | NP_000413.1:n.432+171C>T | |
| NM_000422.3:c.432+171C>T MANE Select | NP_000413.1:n.432+171C>T |