Linked Data
dbSNP Id:
rs17887200
gnomAD v2:
17-7571071-T-C
gnomAD v3:
17-7667753-T-C
gnomAD v4:
17-7667753-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7667753T>C , CM000679.2:g.7667753T>C | GRCh38 |
| NC_000017.10:g.7571071T>C , CM000679.1:g.7571071T>C | GRCh37 |
| NC_000017.9:g.7511796T>C | NCBI36 |
| NG_017013.2:g.24798A>G , LRG_321:g.24798A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000359597.8:c.994-1509A>G | ENSP00000352610.4:n.994-1509A>G | |
| ENST00000413465.6:c.783-5739A>G | ENSP00000410739.2:n.783-5739A>G | |
| ENST00000635293.1:c.984-328A>G | ENSP00000488924.1:n.984-328A>G |