Linked Data
dbSNP Id:
rs1187991466
gnomAD v2:
17-7571634-C-T
gnomAD v3:
17-7668316-C-T
gnomAD v4:
17-7668316-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7668316C>T , CM000679.2:g.7668316C>T | GRCh38 |
| NC_000017.10:g.7571634C>T , CM000679.1:g.7571634C>T | GRCh37 |
| NC_000017.9:g.7512359C>T | NCBI36 |
| NG_017013.2:g.24235G>A , LRG_321:g.24235G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000359597.8:c.994-2072G>A | ENSP00000352610.4:n.994-2072G>A | |
| ENST00000413465.6:c.782+5865G>A | ENSP00000410739.2:n.782+5865G>A | |
| ENST00000635293.1:c.984-891G>A | ENSP00000488924.1:n.984-891G>A |