Linked Data
dbSNP Id:
rs1768157863
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32819185C>T , CM000668.2:g.32819185C>T | GRCh38 |
| NC_000006.11:g.32786962C>T , CM000668.1:g.32786962C>T | GRCh37 |
| NC_000006.10:g.32894940C>T | NCBI36 |
| NG_009793.3:g.24586G>A | |
| NG_012008.1:g.2864G>A | |
| NG_009793.4:g.24586G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648009.1:c.-2+1126G>A | ENSP00000496848.1:n.-2+1126G>A | |
| ENST00000452392.2:c.1933-2233G>A | ENSP00000391806.2:n.1933-2233G>A |