Linked Data
dbSNP Id:
rs1777821810
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151666351A>T , CM000668.2:g.151666351A>T | GRCh38 |
| NC_000006.11:g.151987486A>T , CM000668.1:g.151987486A>T | GRCh37 |
| NC_000006.10:g.152029179A>T | NCBI36 |
| NG_008493.2:g.14661A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000473497.5:n.73+9588A>T | ||
| XM_017010376.1:c.-202+9588A>T | XP_016865865.1:n.-202+9588A>T | |
| XM_017010377.1:c.-260-39A>T | XP_016865866.1:n.-260-39A>T | |
| XM_017010380.1:c.-71+9588A>T | XP_016865869.1:n.-71+9588A>T | |
| NM_001385568.1:c.-202+9588A>T | NP_001372497.1:n.-202+9588A>T |