Linked Data
dbSNP Id:
rs1322178
gnomAD v2:
6-106631780-C-T
gnomAD v3:
6-106183905-C-T
gnomAD v4:
6-106183905-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.106183905C>T , CM000668.2:g.106183905C>T | GRCh38 |
| NC_000006.11:g.106631780C>T , CM000668.1:g.106631780C>T | GRCh37 |
| NC_000006.10:g.106738473C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000636335.1:c.457+18067G>A | ENSP00000490221.1:n.457+18067G>A | |
| ENST00000636437.1:c.457+18067G>A | ENSP00000490376.1:n.457+18067G>A |