Linked Data
dbSNP Id:
rs1316028156
gnomAD v2:
17-4637487-C-T
gnomAD v3:
17-4734192-C-T
gnomAD v4:
17-4734192-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4734192C>T , CM000679.2:g.4734192C>T | GRCh38 |
| NC_000017.10:g.4637487C>T , CM000679.1:g.4637487C>T | GRCh37 |
| NC_000017.9:g.4584236C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293778.12:c.*311G>A MANE Select | ENSP00000293778.7:n.*311G>A | |
| ENST00000293778.10:c.*311G>A | ENSP00000293778.6:n.*311G>A | |
| ENST00000576153.5:n.867G>A | ||
| NM_022059.3:c.*311G>A | NP_071342.2:n.*311G>A | |
| NM_022059.4:c.*311G>A | NP_071342.2:n.*311G>A | |
| NM_001386809.1:c.*311G>A MANE Select | NP_001373738.1:n.*311G>A |