Linked Data
dbSNP Id:
rs1019521961
gnomAD v2:
9-22010012-C-A
gnomAD v3:
9-22010013-C-A
gnomAD v4:
9-22010013-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22010013C>A , CM000671.2:g.22010013C>A | GRCh38 |
| NC_000009.11:g.22010012C>A , CM000671.1:g.22010012C>A | GRCh37 |
| NC_000009.10:g.22000012C>A | NCBI36 |
| NG_023297.1:g.4301G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000404796.3:c.348-19420C>A | ENSP00000385916.2:n.348-19420C>A | |
| ENST00000404796.2:c.348-19420C>A | ENSP00000385916.2:n.348-19420C>A | |
| NR_003529.3:n.371+14852C>A | ||
| NR_047532.1:n.371+14852C>A | ||
| NR_047533.1:n.371+14852C>A | ||
| NR_047534.1:n.371+14852C>A | ||
| NR_047535.1:n.371+14852C>A | ||
| NR_047536.1:n.371+14852C>A | ||
| NR_047537.1:n.371+14852C>A | ||
| NR_047538.1:n.371+14852C>A | ||
| NR_047539.1:n.371+14852C>A | ||
| NR_047540.1:n.371+14852C>A | ||
| NR_047541.1:n.371+14852C>A | ||
| NR_047542.1:n.371+14852C>A | ||
| NR_047543.1:n.371+14852C>A | ||
| NR_120536.1:n.371+14852C>A |